| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
45A A clinical events system with committee review for a large clinical trials network
|
Green, Lisa A.
|
|
1995
|
16 |
3S1 |
p. 58S-59S
nvt p.
|
artikel
|
| 2 |
01A A comparison of the performance of several phase I designs
|
Odom-Maryon, Tamara
|
|
1995
|
16 |
3S1 |
p. 33S-
1 p.
|
artikel
|
| 3 |
34A Adjusting estimates of a laboratory parameter effect in a neonatal study based on center differences in a multi-center
|
Boardman, Chris
|
|
1995
|
16 |
3S1 |
p. 52S-
1 p.
|
artikel
|
| 4 |
57A A graphical assessment of the potential impact of losses to followup on the validity of study results
|
Matts, John P.
|
|
1995
|
16 |
3S1 |
p. 65S-66S
nvt p.
|
artikel
|
| 5 |
62A A meta-analysis of clinical trials involving both continuous and binary outcomes
|
Whitehead, Anne
|
|
1995
|
16 |
3S1 |
p. 68S-
1 p.
|
artikel
|
| 6 |
30A Analysis on clinical signs and symptoms of antimicrobial trials
|
Yang, Joanna
|
|
1995
|
16 |
3S1 |
p. 50S-
1 p.
|
artikel
|
| 7 |
68A Analyzing multiple endpoints from multiple time periods with multiple groups: The PEPI cohort
|
Legault, Claudine
|
|
1995
|
16 |
3S1 |
p. 71S-
1 p.
|
artikel
|
| 8 |
51A Applying the “real-time meta-analysis system” to randomized control trials of congestive heart failure
|
Cappelleri, Joseph C.
|
|
1995
|
16 |
3S1 |
p. 62S-
1 p.
|
artikel
|
| 9 |
54A A randomized trial with surgery as the manoeuvre and endpoint
|
Kestle, J.
|
|
1995
|
16 |
3S1 |
p. 64S-
1 p.
|
artikel
|
| 10 |
27A Are clinical trial participants comparable to non-participants?
|
Weijer, Charles
|
|
1995
|
16 |
3S1 |
p. 48S-
1 p.
|
artikel
|
| 11 |
21A Are we promoting a true informed consent for participation in randomized clinical trials?
|
DeLuca, Sue A.
|
|
1995
|
16 |
3S1 |
p. 44S-
1 p.
|
artikel
|
| 12 |
09A Assessing medication adherence in the African American study of kidney disease and hypertension (AASK) pilot study
|
Lee, Jeannette
|
|
1995
|
16 |
3S1 |
p. 37S-
1 p.
|
artikel
|
| 13 |
36A Assessing neurodevelopment in pediatric HIV patients
|
Rutkiewicz, Victoria
|
|
1995
|
16 |
3S1 |
p. 53S-
1 p.
|
artikel
|
| 14 |
46A A survey of data entry methods: Substituting data for “religion”
|
Singer, Stephen W.
|
|
1995
|
16 |
3S1 |
p. 59S-
1 p.
|
artikel
|
| 15 |
38A Benefit-risk ratios in the assessment of the clinical evidence of a new therapy
|
Willan, Andrew R.
|
|
1995
|
16 |
3S1 |
p. 54S-
1 p.
|
artikel
|
| 16 |
48A Benefits of a centralized clinical trials data management system
|
Matza, Martha J.
|
|
1995
|
16 |
3S1 |
p. 60S-
1 p.
|
artikel
|
| 17 |
19A Challenge of minority recruitment in clinical trials: Experience of the African American study of kidney disease and hypertension (AASK) pilot study
|
Whelton, Paul
|
|
1995
|
16 |
3S1 |
p. 43S-
1 p.
|
artikel
|
| 18 |
24A Challenges of a large simple trial: The Zerit® parallel track
|
Brunell, Robert
|
|
1995
|
16 |
3S1 |
p. 46S-
1 p.
|
artikel
|
| 19 |
65A Chaos theory and prognosis: Selection of patients with arrhythmias and an increased risk of sudden cardiac death
|
Ulm, K.
|
|
1995
|
16 |
3S1 |
p. 70S-
1 p.
|
artikel
|
| 20 |
17A Clinical trial participant satisfaction: Survey of 4281 participants in the systolic hypertension in the elderly program
|
Schron, Eleanor B.
|
|
1995
|
16 |
3S1 |
p. 41S-42S
nvt p.
|
artikel
|
| 21 |
28A Comparison of median survival times with adjustment for covariates
|
Karrison, Theodore
|
|
1995
|
16 |
3S1 |
p. 48S-49S
nvt p.
|
artikel
|
| 22 |
22A Comparison of methods for health economic measurements in clinical trials
|
Walker, Valery
|
|
1995
|
16 |
3S1 |
p. 45S-
1 p.
|
artikel
|
| 23 |
56A Comparison of time-to-event and slope-based analyses in nephrology clinical trials
|
Greene, Tom
|
|
1995
|
16 |
3S1 |
p. 65S-
1 p.
|
artikel
|
| 24 |
02A Considerations in designing pediatric drug trials
|
Simpson, Pippa
|
|
1995
|
16 |
3S1 |
p. 33S-
1 p.
|
artikel
|
| 25 |
26A Coronary revascularization practice in the 1990s is it different at academic centers?
|
Rosen, Allan D.
|
|
1995
|
16 |
3S1 |
p. 47S-48S
nvt p.
|
artikel
|
| 26 |
23A Cost-effectiveness analysis in the V.A. Cooperative Study of transurethral resection of the prostate vs. watchful waiting in benign prostatic hyperplasia
|
Henderson, William
|
|
1995
|
16 |
3S1 |
p. 45S-46S
nvt p.
|
artikel
|
| 27 |
50A Critical events management
|
Viséle, Nathalie
|
|
1995
|
16 |
3S1 |
p. 61S-62S
nvt p.
|
artikel
|
| 28 |
35A Defining and analyzing asthma exacerbation
|
Zhang, Ji
|
|
1995
|
16 |
3S1 |
p. 52S-
1 p.
|
artikel
|
| 29 |
67A Designed extension of studies based on conditional power
|
Proschan, Michael A.
|
|
1995
|
16 |
3S1 |
p. 71S-
1 p.
|
artikel
|
| 30 |
43A Did blinding work in a trial of lipid-lowering and low-dose anticoagulant agents?
|
Margitic, Susan
|
|
1995
|
16 |
3S1 |
p. 57S-
1 p.
|
artikel
|
| 31 |
52A Effectiveness of a placebo run-in period in increasing the power of a chemoprevention trial, CARET
|
Thornquist, Mark
|
|
1995
|
16 |
3S1 |
p. 63S-
1 p.
|
artikel
|
| 32 |
11A Electronic document archival for a data coordinating center
|
Wong, Kenneth
|
|
1995
|
16 |
3S1 |
p. 38S-
1 p.
|
artikel
|
| 33 |
32A Estimating rate of change in lumbar spine bone mineral density in clinical trials for treatments of osteoporosis
|
Yuan, Weiying
|
|
1995
|
16 |
3S1 |
p. 51S-
1 p.
|
artikel
|
| 34 |
06A From clinical trial to bedside: Enhancing patient care through the use of continuous quality improvement techniques
|
Ackman, Margaret L.
|
|
1995
|
16 |
3S1 |
p. 35S-
1 p.
|
artikel
|
| 35 |
07A How do clinic coordinators spend their time?
|
Church, Renee Y.
|
|
1995
|
16 |
3S1 |
p. 36S-
1 p.
|
artikel
|
| 36 |
33A How we used graphics in the Lung Health Study
|
Connett, John E.
|
|
1995
|
16 |
3S1 |
p. 51S-
1 p.
|
artikel
|
| 37 |
41A Impact of trial results on clinical practice one year following the systolic hypertension in the elderly program
|
Herzog, Holly C.
|
|
1995
|
16 |
3S1 |
p. 56S-
1 p.
|
artikel
|
| 38 |
39A Incorporating toxicity grade information in the continual reassessment method for phase I cancer clinical trials
|
de Moor, Carl A.
|
|
1995
|
16 |
3S1 |
p. 54S-55S
nvt p.
|
artikel
|
| 39 |
13A Information-based monitoring and design of time to event studies
|
Scharfstein, Daniel O.
|
|
1995
|
16 |
3S1 |
p. 39S-
1 p.
|
artikel
|
| 40 |
12A Interactive database management (IDM)
|
Othman, R.O.
|
|
1995
|
16 |
3S1 |
p. 38S-39S
nvt p.
|
artikel
|
| 41 |
64A Investigating the stability of patient classification into risk groups: An example in Crohn's disease
|
Sahmoud, Tarek
|
|
1995
|
16 |
3S1 |
p. 69S-
1 p.
|
artikel
|
| 42 |
04A Legislative oversight of clinical trials
|
Kane, Christopher D.
|
|
1995
|
16 |
3S1 |
p. 34S-
1 p.
|
artikel
|
| 43 |
58A Measuring the impact of the control rate in meta-analysis of clinical trials
|
Schmid, Christopher H.
|
|
1995
|
16 |
3S1 |
p. 66S-
1 p.
|
artikel
|
| 44 |
60A Ovarian ablation — Why the Early Breast Cancer Trialists' Collaborative Group's (EBCTCG) individual patient data meta-analysis was needed
|
Clarke, Mike
|
|
1995
|
16 |
3S1 |
p. 67S-68S
nvt p.
|
artikel
|
| 45 |
15A Paternal cell immunization for recurrent miscarriage: A comparison of meta-analyses with and without individual patient data
|
Jeng, Gary T.
|
|
1995
|
16 |
3S1 |
p. 40S-
1 p.
|
artikel
|
| 46 |
69A Performance of the National Death Index and probabilistic decision rules for reducing the number of false matches
|
Kosinski, Andrzej S.
|
|
1995
|
16 |
3S1 |
p. 72S-
1 p.
|
artikel
|
| 47 |
14A Publication and reporting of phase I clinical trials
|
Winget, Marcy
|
|
1995
|
16 |
3S1 |
p. 40S-
1 p.
|
artikel
|
| 48 |
37A Quality of life measurement in an HIV-clinical trial
|
Messina, Marianne
|
|
1995
|
16 |
3S1 |
p. 53S-54S
nvt p.
|
artikel
|
| 49 |
66A Randomized and non-randomized patients in clinical trials: Experiences with comprehensive cohort studies
|
Sauerbrei, W.
|
|
1995
|
16 |
3S1 |
p. 70S-71S
nvt p.
|
artikel
|
| 50 |
53A Randomize the first patient? Benefits and risks of adding a new treatment-arm to a longterm clinical trial
|
Hasford, Joerg
|
|
1995
|
16 |
3S1 |
p. 63S-64S
nvt p.
|
artikel
|
| 51 |
18A Reasons for joining and barriers to participation in the African-American study of kidney disease and hypertension (AASK) pilot study
|
Kusek, John
|
|
1995
|
16 |
3S1 |
p. 42S-
1 p.
|
artikel
|
| 52 |
55A Role for clinical databases and risk adjustment in clinical trial analytic plans
|
Knaus, W.A.
|
|
1995
|
16 |
3S1 |
p. 64S-65S
nvt p.
|
artikel
|
| 53 |
49A Standard interface to a clinical trials data management system
|
Welch, Susan Rea
|
|
1995
|
16 |
3S1 |
p. 61S-
1 p.
|
artikel
|
| 54 |
08A TermPROM coordinator survey
|
Hewson, Sheila
|
|
1995
|
16 |
3S1 |
p. 36S-
1 p.
|
artikel
|
| 55 |
25A The antihypertensive and lipid lowering treatment to prevent heart attack trial: Design features
|
Davis, Barry R.
|
|
1995
|
16 |
3S1 |
p. 47S-
1 p.
|
artikel
|
| 56 |
42A The effect of long-term treatment with oral anticoagulants on mortality and cardiovascular morbidity after myocardial infarction
|
Azar, Aida J.
|
|
1995
|
16 |
3S1 |
p. 56S-57S
nvt p.
|
artikel
|
| 57 |
59A The fallacy of the analysis of treatment effect according to the control group rates in systematic reviews
|
Torri, V.
|
|
1995
|
16 |
3S1 |
p. 67S-
1 p.
|
artikel
|
| 58 |
40A The identification of predictive factors of missing follow-up in GISSI-3 trial
|
Bonfanti, E.
|
|
1995
|
16 |
3S1 |
p. 55S-
1 p.
|
artikel
|
| 59 |
20A The impact of simultaneous participation on two large multicentre, multinational clinical trials
|
Fabri, Jackie
|
|
1995
|
16 |
3S1 |
p. 43S-44S
nvt p.
|
artikel
|
| 60 |
05A The international register of RCTS of health care
|
Dickersin, Kay
|
|
1995
|
16 |
3S1 |
p. 35S-
1 p.
|
artikel
|
| 61 |
16A The use of incentives to increase participation in a chemoprevention trial
|
Bowen, Deborah
|
|
1995
|
16 |
3S1 |
p. 41S-
1 p.
|
artikel
|
| 62 |
29A The use of Poisson regression methods in clinical trials
|
Thompson, Desmond
|
|
1995
|
16 |
3S1 |
p. 49S-
1 p.
|
artikel
|
| 63 |
31A Tracking in random regression mixed models for longitudinal data: Graphical examination and comparison of BLUP and OLS procedures
|
Helms, Ronald W.
|
|
1995
|
16 |
3S1 |
p. 50S-
1 p.
|
artikel
|
| 64 |
44A Treatment effects monitoring practices as viewed through the published literature
|
Kiri, Antariksha
|
|
1995
|
16 |
3S1 |
p. 58S-
1 p.
|
artikel
|
| 65 |
10A Use of the internet in coordinating information from clinical centers and a central laboratory in the Mortality and Morbidity in Hemodialysis (MMHD) study
|
Drabik, M.
|
|
1995
|
16 |
3S1 |
p. 37S-38S
nvt p.
|
artikel
|
| 66 |
61A User requirements for the meta-analysis of individual patient data
|
Sylvester, Richard
|
|
1995
|
16 |
3S1 |
p. 68S-
1 p.
|
artikel
|
| 67 |
Author index
|
|
|
1995
|
16 |
3S1 |
p. 142S-158S
nvt p.
|
artikel
|
| 68 |
63A Utilizing sequential monitoring boundaries for cumulative meta-analysis
|
Pogue, Janice
|
|
1995
|
16 |
3S1 |
p. 69S-
1 p.
|
artikel
|
| 69 |
47A Validation of computer systems for clinical trials — Experiences with a practical implementation
|
Brandmaier, Roland
|
|
1995
|
16 |
3S1 |
p. 60S-
1 p.
|
artikel
|
| 70 |
03A Visit windows and drug supplies
|
Guidarelli, Loretta A.
|
|
1995
|
16 |
3S1 |
p. 34S-
1 p.
|
artikel
|
| 71 |
Calendar of program
|
|
|
1995
|
16 |
3S1 |
p. 3S-31S
nvt p.
|
artikel
|
| 72 |
Letter from the President
|
|
|
1995
|
16 |
3S1 |
p. 1S-
1 p.
|
artikel
|
| 73 |
P31 A bayesian belief network for exploratory longitudinal analysis
|
Clarke, Ellis
|
|
1995
|
16 |
3S1 |
p. 89S-90S
nvt p.
|
artikel
|
| 74 |
P116 A comparison of APACHE II (Acute Physiology And Chronic Health Evaluation score) and MODS (Multiple Organ Dysfunction Score) in predicting ICU mortality
|
Griffith, Lauren
|
|
1995
|
16 |
3S1 |
p. 138S-
1 p.
|
artikel
|
| 75 |
P06 A comparison of key data entry versus FAX data entry, accuracy and time
|
Lancaster, Scott
|
|
1995
|
16 |
3S1 |
p. 75S-76S
nvt p.
|
artikel
|
| 76 |
P55 A comparison of medical abstraction and physician review of hospital records in the lung health study
|
Lee, Wondra Wong
|
|
1995
|
16 |
3S1 |
p. 104S-
1 p.
|
artikel
|
| 77 |
P37 A comparison of methods used to summarize responses on the Functional Status Questionnaire (FSQ) unscaled responses vs scaled scores
|
Randall, A.M.Y.
|
|
1995
|
16 |
3S1 |
p. 93S-
1 p.
|
artikel
|
| 78 |
P11 A complex data editing system utilizing Structured Query Language (SQL)
|
Jones, Martha F.
|
|
1995
|
16 |
3S1 |
p. 78S-79S
nvt p.
|
artikel
|
| 79 |
P09 A data collection system designed to facilitate participation in multiple concurrent clinical trials
|
Wentworth, Deborah
|
|
1995
|
16 |
3S1 |
p. 77S-
1 p.
|
artikel
|
| 80 |
P10 A data management tool for tracking clinical endpoint reviews
|
Myers, Marcella
|
|
1995
|
16 |
3S1 |
p. 78S-
1 p.
|
artikel
|
| 81 |
P25 Age, sex, and race in ophthalmology randomized clinical trials
|
Crawley, Barbara
|
|
1995
|
16 |
3S1 |
p. 86S-
1 p.
|
artikel
|
| 82 |
P110 Analyses of repeated measurements data from two treatment groups
|
Huang, David C.
|
|
1995
|
16 |
3S1 |
p. 135S-
1 p.
|
artikel
|
| 83 |
P16 An automated editing process for research databases
|
Moke, Pamela S.
|
|
1995
|
16 |
3S1 |
p. 81S-
1 p.
|
artikel
|
| 84 |
P70 An electronic interface for reporting and tracking significant clinical events
|
Pelusio, Rita M.
|
|
1995
|
16 |
3S1 |
p. 112S-113S
nvt p.
|
artikel
|
| 85 |
P29 An evaluation of methods for sensitivity and specificity when the observations are correlated
|
Ahn, Chul
|
|
1995
|
16 |
3S1 |
p. 88S-89S
nvt p.
|
artikel
|
| 86 |
P92 Angiographic eligibility assessment in the bypass angioplasty revascularization investigation
|
Wisniewski, Stephen R.
|
|
1995
|
16 |
3S1 |
p. 124S-125S
nvt p.
|
artikel
|
| 87 |
P19 An integrated system for meta-analyses of individual patient data: Data dictionary and database structure
|
Bijnens, Luc
|
|
1995
|
16 |
3S1 |
p. 82S-83S
nvt p.
|
artikel
|
| 88 |
P94 A one page daily calendar as an aid in tracking variables in clinical trials
|
Wilkins, Annette
|
|
1995
|
16 |
3S1 |
p. 125S-126S
nvt p.
|
artikel
|
| 89 |
P23 Appending a cost-effectiveness analysis to a randomized trial of laparoscopic surgery
|
Gray, Darryl
|
|
1995
|
16 |
3S1 |
p. 85S-
1 p.
|
artikel
|
| 90 |
P34 Applying cause-specific failure endpoint analysis strategies
|
Panzarella, Tony
|
|
1995
|
16 |
3S1 |
p. 91S-
1 p.
|
artikel
|
| 91 |
P46 A protocol to minimize bias and regression to the mean in measurement of intraocular pressure
|
Gordon, Mae O.
|
|
1995
|
16 |
3S1 |
p. 98S-99S
nvt p.
|
artikel
|
| 92 |
P48 A quality control study of radionuclide ventriculogram readings of left ventricular ejection fraction without using a core lab
|
Bost, James E.
|
|
1995
|
16 |
3S1 |
p. 100S-
1 p.
|
artikel
|
| 93 |
P115 A review of recent statistical methods for the analysis of the 2x2 crossover design in clinical trials
|
Stepanavage, Michael
|
|
1995
|
16 |
3S1 |
p. 137S-
1 p.
|
artikel
|
| 94 |
P76 A SAS macro to perform the randomization test alternative to the dependent samples t-test
|
Foster, Gary A.
|
|
1995
|
16 |
3S1 |
p. 115S-116S
nvt p.
|
artikel
|
| 95 |
P83 A sequential design to assess the efficacy of dry polymer gel pads during mayor surgery
|
McElvenny, Damien
|
|
1995
|
16 |
3S1 |
p. 119S-120S
nvt p.
|
artikel
|
| 96 |
P81 A trial evaluating the home treatment of patients with acute proximal deep vein thrombosis (DVT)
|
Haley, Susan
|
|
1995
|
16 |
3S1 |
p. 118S-
1 p.
|
artikel
|
| 97 |
P106 A useful management technique for monitoring the progress of large multi-national clinical trials
|
Karnash, Sharon
|
|
1995
|
16 |
3S1 |
p. 133S-
1 p.
|
artikel
|
| 98 |
P64 Automated generation of program code and documentation for database error checking
|
Connorton, Joseph
|
|
1995
|
16 |
3S1 |
p. 109S-
1 p.
|
artikel
|
| 99 |
P72 A windows interface to a relational database for data management
|
Jones, Martha F.
|
|
1995
|
16 |
3S1 |
p. 113S-114S
nvt p.
|
artikel
|
| 100 |
P88 Barriers encountered in the conduct of clinical studies: A case in point. Perioperatively discontinuation of MTX
|
Alarcón, Graciela S.
|
|
1995
|
16 |
3S1 |
p. 122S-123S
nvt p.
|
artikel
|
| 101 |
P03 Being prepared: A case study
|
Remaley, Nancy
|
|
1995
|
16 |
3S1 |
p. 74S-
1 p.
|
artikel
|
| 102 |
P05 Beyond intra-form and inter-form editing: Inter-study editing and quality assurance
|
Eng, Heather
|
|
1995
|
16 |
3S1 |
p. 75S-
1 p.
|
artikel
|
| 103 |
P90 Biologic variability in the evaluation of osteoporosis
|
Simpson, Pippa
|
|
1995
|
16 |
3S1 |
p. 123S-
1 p.
|
artikel
|
| 104 |
P96 Biostatistical/clinical issues in global drug development
|
Herson, Jay
|
|
1995
|
16 |
3S1 |
p. 127S-
1 p.
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artikel
|
| 105 |
P42 Blinding and exclusions after randomization in controlled trials
|
Schulz, Kenneth F.
|
|
1995
|
16 |
3S1 |
p. 95S-96S
nvt p.
|
artikel
|
| 106 |
P12 Blueprint for a data collection tool
|
Hewson, Sheila
|
|
1995
|
16 |
3S1 |
p. 79S-
1 p.
|
artikel
|
| 107 |
P108 Central measurement of comorbidity and local measurement of functional status and quality of life in the mortality and morbidity in hemodialysis (MMHD) Pilot Study
|
Gassman, Jennifer
|
|
1995
|
16 |
3S1 |
p. 134S-
1 p.
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artikel
|
| 108 |
P73 Clinical site staff turnover: Effective training approaches in a multi-center clinical trial
|
Crow, Sharon
|
|
1995
|
16 |
3S1 |
p. 114S-
1 p.
|
artikel
|
| 109 |
P61 Closeout issues in a permanently implantable investigational device study
|
Morgan, Nancy
|
|
1995
|
16 |
3S1 |
p. 108S-
1 p.
|
artikel
|
| 110 |
P63 Communication procedures for on-going clinical trials
|
Nowakowski, Deborah J.
|
|
1995
|
16 |
3S1 |
p. 109S-
1 p.
|
artikel
|
| 111 |
P107 Comparison of inevaluability rates between community and comprehensive center investigators
|
Winn, Rodger J.
|
|
1995
|
16 |
3S1 |
p. 133S-134S
nvt p.
|
artikel
|
| 112 |
P100 Comparison of tablet measures by calibrated cylinder versus tablet count in the DIG study
|
Fye, Carol L.
|
|
1995
|
16 |
3S1 |
p. 129S-
1 p.
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artikel
|
| 113 |
P08 Computer aided telephone screening and recruitment via in-house developed PC FoxPro application
|
Little, Angela
|
|
1995
|
16 |
3S1 |
p. 77S-
1 p.
|
artikel
|
| 114 |
P85 Considerations regarding “measurement visits” during follow up of clinical trials
|
Paranandi, Lata
|
|
1995
|
16 |
3S1 |
p. 120S-121S
nvt p.
|
artikel
|
| 115 |
P57 Coordinating recruitment in the Women's Health Initiative
|
Hunt, Julie R.
|
|
1995
|
16 |
3S1 |
p. 105S-
1 p.
|
artikel
|
| 116 |
P86 Cost analysis in clinical trials
|
Wisniewski, Stephen R.
|
|
1995
|
16 |
3S1 |
p. 121S-
1 p.
|
artikel
|
| 117 |
P38 Data analysis plan development in a changing environment
|
Capizzi, Thomas
|
|
1995
|
16 |
3S1 |
p. 93S-94S
nvt p.
|
artikel
|
| 118 |
P13 Data dictionary driven export of a relational data base to SAS data sets
|
Paulsen, Jay M.
|
|
1995
|
16 |
3S1 |
p. 79S-80S
nvt p.
|
artikel
|
| 119 |
P04 Data management considerations for the HIVNET clinical trials
|
Williams, Allan E.
|
|
1995
|
16 |
3S1 |
p. 74S-75S
nvt p.
|
artikel
|
| 120 |
P65 Data management issues in angiographic core laboratory data in coronary studies
|
Kennard, Elizabeth D.
|
|
1995
|
16 |
3S1 |
p. 110S-
1 p.
|
artikel
|
| 121 |
P112 Decision tree analysis: Application in diagnosing hemodynamically severe carotid stenosis
|
Reed III, J.F.
|
|
1995
|
16 |
3S1 |
p. 136S-
1 p.
|
artikel
|
| 122 |
P40 Design and analysis of clinical trials via sequential conditional probability ration test
|
Ming, Tan
|
|
1995
|
16 |
3S1 |
p. 94S-95S
nvt p.
|
artikel
|
| 123 |
P67 Design and implementation of a computerized system for a colon cancer prevention program
|
Lin, K.
|
|
1995
|
16 |
3S1 |
p. 111S-
1 p.
|
artikel
|
| 124 |
P68 Design and implementation of a patient tracking system for the Ontario trial of active compression-decompression cardiopulmonary resuscitation (OTAC)
|
Campbell-Daigle, Fiona
|
|
1995
|
16 |
3S1 |
p. 111S-112S
nvt p.
|
artikel
|
| 125 |
P49 Designing standard reports for a clinical research database
|
Marks, Linda D.
|
|
1995
|
16 |
3S1 |
p. 100S-101S
nvt p.
|
artikel
|
| 126 |
P98 Design of a phase III trial of cryptococcal meningitis in AIDS patients
|
Cloud, Gretchen
|
|
1995
|
16 |
3S1 |
p. 128S-
1 p.
|
artikel
|
| 127 |
P84 Drop-outs and drop-ins in a clinical trial of a lipid-lowering agent
|
Byington, Robert P.
|
|
1995
|
16 |
3S1 |
p. 120S-
1 p.
|
artikel
|
| 128 |
P45 Effects of rapid accrual on interim safety and efficacy monitoring: The minocycline in rheumatoid arthritis (MIRA) trial
|
Fowler, Sarah
|
|
1995
|
16 |
3S1 |
p. 98S-
1 p.
|
artikel
|
| 129 |
P80 Electronic documentation for validation of statistical analysis programming for data from clinical trials
|
Bell, Margie
|
|
1995
|
16 |
3S1 |
p. 117S-118S
nvt p.
|
artikel
|
| 130 |
P103 Establishing normative values of public health for outcomes based research
|
Wasser, T.E.
|
|
1995
|
16 |
3S1 |
p. 131S-
1 p.
|
artikel
|
| 131 |
P117 Estimation of treatment effect and its resolution using a two-phase mixed model
|
Wei, Lynn
|
|
1995
|
16 |
3S1 |
p. 138S-139S
nvt p.
|
artikel
|
| 132 |
P113 Evaluating interrater agreement based on categorical scales
|
Kotey, Paul
|
|
1995
|
16 |
3S1 |
p. 136S-
1 p.
|
artikel
|
| 133 |
P01 Evaluating the benefits of patient video during the informed consent process
|
Weston, J.
|
|
1995
|
16 |
3S1 |
p. 73S-
1 p.
|
artikel
|
| 134 |
P30 Experience with multivariate survival analysis for clinical trials
|
Van Natta, Mark L.
|
|
1995
|
16 |
3S1 |
p. 89S-
1 p.
|
artikel
|
| 135 |
P32 Experience with preplanned meta analyses in linked clinical trials aimed at reducing frailty in older adults
|
Schechtman, Kenneth B.
|
|
1995
|
16 |
3S1 |
p. 90S-
1 p.
|
artikel
|
| 136 |
P24 Factors in successful patient recruitment applying the six-box organizational model in a large VA cooperative study
|
Collins, Dorothea
|
|
1995
|
16 |
3S1 |
p. 85S-86S
nvt p.
|
artikel
|
| 137 |
P97 Fast tracking with master contracts
|
Brown, Philip M.
|
|
1995
|
16 |
3S1 |
p. 127S-
1 p.
|
artikel
|
| 138 |
P78 Forecasting enrollment capacity in a cooperative clinical trial network
|
Shen, Wei
|
|
1995
|
16 |
3S1 |
p. 116S-117S
nvt p.
|
artikel
|
| 139 |
P41 Graphical display of three dimensional compositional data using a ternary diagram
|
Nguyen, Ha H.
|
|
1995
|
16 |
3S1 |
p. 95S-
1 p.
|
artikel
|
| 140 |
P114 Graphical presentation of longitudinal data analyses: The nhlbi growth and health study (NGHS)
|
Similo, Shari L.
|
|
1995
|
16 |
3S1 |
p. 137S-
1 p.
|
artikel
|
| 141 |
P44 Implementation of multicenter clinical trials: The Alzheimer's Disease Cooperative Study protocol implementation manual
|
Schafer, Kimberly
|
|
1995
|
16 |
3S1 |
p. 97S-
1 p.
|
artikel
|
| 142 |
P91 Improved readability of consent forms for clinical trials
|
Sadura, Anna
|
|
1995
|
16 |
3S1 |
p. 124S-
1 p.
|
artikel
|
| 143 |
P07 Information system for a multi-hospital study using optical scanning and hospital database downloads
|
Anderson, Stephen
|
|
1995
|
16 |
3S1 |
p. 76S-
1 p.
|
artikel
|
| 144 |
P59 Informed consent vs. randomized consent: A randomized trial with healthy subjects
|
Gallo, Ciro
|
|
1995
|
16 |
3S1 |
p. 106S-107S
nvt p.
|
artikel
|
| 145 |
P26 Initiating a clinical trial utilizing project management software: A pharmacy perspective
|
Peterson, Jenine C.
|
|
1995
|
16 |
3S1 |
p. 86S-87S
nvt p.
|
artikel
|
| 146 |
P74 Insuring data completeness from multiple data sources
|
Gross, Richard D.
|
|
1995
|
16 |
3S1 |
p. 114S-
1 p.
|
artikel
|
| 147 |
P17 Issues in using a university data coordinating center for an industry sponsored clinical trial
|
Barnhart, Murray D.
|
|
1995
|
16 |
3S1 |
p. 81S-
1 p.
|
artikel
|
| 148 |
P33 Longitudinal analysis of binary data in the V.A. cooperative study of sulfasalazine for the treatment of seronegative spondyloarthropathies
|
Reda, Domenic
|
|
1995
|
16 |
3S1 |
p. 90S-91S
nvt p.
|
artikel
|
| 149 |
P35 Longitudinal study of cardinal features of cognitive dysfunction in alzheimer's disease
|
Talwalker, Sheela
|
|
1995
|
16 |
3S1 |
p. 92S-
1 p.
|
artikel
|
| 150 |
P105 Maintenance of adherence to a dietary intervention 9 months after completion of a clinical trial
|
Kusek, John
|
|
1995
|
16 |
3S1 |
p. 132S-
1 p.
|
artikel
|
| 151 |
P102 Methods to promote staff retention in a large, multi-site chemoprevention study: The caret experience
|
Powell, Corinne
|
|
1995
|
16 |
3S1 |
p. 130S-
1 p.
|
artikel
|
| 152 |
P71 Migration of statistical processing across operating systems
|
Pollizzi, Susan
|
|
1995
|
16 |
3S1 |
p. 113S-
1 p.
|
artikel
|
| 153 |
P111 Missing data imputation for continuous outcome measures: The dietary intervention study in children (DISC)
|
McMahon, Robert P.
|
|
1995
|
16 |
3S1 |
p. 135S-
1 p.
|
artikel
|
| 154 |
P14 Monitoring data error rates: A tool for maintaining high standards in data quality
|
Lawlor, Sharon
|
|
1995
|
16 |
3S1 |
p. 80S-
1 p.
|
artikel
|
| 155 |
P54 Ninety-nine percent patient follow-up in a large clinical trial: A five step plan
|
Davis, Catherine G.
|
|
1995
|
16 |
3S1 |
p. 103S-104S
nvt p.
|
artikel
|
| 156 |
P82 Objective classification of clinical events in large clinical trials: Is it worth the cost?
|
Granger, Christopher
|
|
1995
|
16 |
3S1 |
p. 119S-
1 p.
|
artikel
|
| 157 |
P79 Outcome research in angina pectoris: Limitations of some phase III trials
|
Ahn, Sylvie
|
|
1995
|
16 |
3S1 |
p. 117S-
1 p.
|
artikel
|
| 158 |
P60 Patient satisfaction with a dietary intervention: The modification of diet in renal disease study
|
Olson, Marian
|
|
1995
|
16 |
3S1 |
p. 107S-
1 p.
|
artikel
|
| 159 |
P95 Planning for long-term storage and retrieval of clinical trial specimens: The postmenopausal estrogen/progestin intervention (PEPI) trial
|
Wasilauskas, Carol H.
|
|
1995
|
16 |
3S1 |
p. 126S-
1 p.
|
artikel
|
| 160 |
P119 Protecting rights of patients, sites, investigators and sponsors while facilitating timely trial initiation
|
Herr, Barbara
|
|
1995
|
16 |
3S1 |
p. 139S-140S
nvt p.
|
artikel
|
| 161 |
P21 Quality control in clinical trials: Protocol compliance auditing
|
Templeton, M.A.
|
|
1995
|
16 |
3S1 |
p. 83S-84S
nvt p.
|
artikel
|
| 162 |
P104 Quality of life data collected before and after randomization
|
Brooks, Maria Mori
|
|
1995
|
16 |
3S1 |
p. 131S-132S
nvt p.
|
artikel
|
| 163 |
P47 Randomized controlled trial of aerobic plus resistance exercise training in patients with congestive heart failure
|
Teo, Koon
|
|
1995
|
16 |
3S1 |
p. 99S-
1 p.
|
artikel
|
| 164 |
P58 Recruitment success by type of site in the antihypertensive and lipid lowering treatment to prevent heart attack trial (ALLHAT) vanguard
|
Egan, Debra A.
|
|
1995
|
16 |
3S1 |
p. 106S-
1 p.
|
artikel
|
| 165 |
P22 Reporting of treatment allocation methods and determinants of sample size in multicenter trials
|
Cramer, Laura D.
|
|
1995
|
16 |
3S1 |
p. 84S-
1 p.
|
artikel
|
| 166 |
P28 Response criteria in solid tumours: UNI-dimensional vs BI-dimensional measurements
|
Muldal, Alison
|
|
1995
|
16 |
3S1 |
p. 88S-
1 p.
|
artikel
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| 167 |
P56 Retention plans in the Women's Health Initiative
|
Bowen, Deborah
|
|
1995
|
16 |
3S1 |
p. 104S-105S
nvt p.
|
artikel
|
| 168 |
P27 Review of measurement, assessment, analysis and reporting of visual acuity in clinical trials in ophthalmology
|
Kiri, Nandini
|
|
1995
|
16 |
3S1 |
p. 87S-
1 p.
|
artikel
|
| 169 |
P43 Rises in the CD4 cell count prior to anti-HIV treatment: Consequences for trial design?
|
Weverling, Gerrit J.
|
|
1995
|
16 |
3S1 |
p. 96S-97S
nvt p.
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artikel
|
| 170 |
P69 Role of Remote Database Management (RDM) as a quality assurance tool: The tone experience
|
Lane, Kathy R.
|
|
1995
|
16 |
3S1 |
p. 112S-
1 p.
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artikel
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| 171 |
P66 SAS® macro routines for the monitoring and the analysis of studies requiring prolonged follow-up
|
Tinazzi, A.
|
|
1995
|
16 |
3S1 |
p. 110S-111S
nvt p.
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artikel
|
| 172 |
P39 Selection of appropriate controls for comparison of survival curves with time-dependent events
|
Forman, Sandra
|
|
1995
|
16 |
3S1 |
p. 94S-
1 p.
|
artikel
|
| 173 |
P99 Selection of clinical sites for the antihypertensive and lipid-lowering treatment to prevent heart attack trial (ALLHAT)
|
Pressel, Sara
|
|
1995
|
16 |
3S1 |
p. 128S-129S
nvt p.
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artikel
|
| 174 |
P18 Strang National High Risk Breast Registry (NHRR) database: Systems architecture and data normalization for long-term research
|
Potter, Charles
|
|
1995
|
16 |
3S1 |
p. 82S-
1 p.
|
artikel
|
| 175 |
P51 Subject enrollment rates in multicenter drug trials: An examination of causes and effects
|
Barnhill, Jamie G.
|
|
1995
|
16 |
3S1 |
p. 101S-102S
nvt p.
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artikel
|
| 176 |
P75 Survey to evaluate case report forms for national multi-center clinical trials designed using genetic forms module
|
Koski, Beverly
|
|
1995
|
16 |
3S1 |
p. 115S-
1 p.
|
artikel
|
| 177 |
P36 Tests useful in situations where treatments increase variability relative to controls
|
Blair, R.Clifford
|
|
1995
|
16 |
3S1 |
p. 92S-93S
nvt p.
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artikel
|
| 178 |
P53 The changing role of informed consent
|
Brown, Philip M.
|
|
1995
|
16 |
3S1 |
p. 103S-
1 p.
|
artikel
|
| 179 |
P87 The cost of screening patients for a randomized clinical trial in orthodontics
|
Philips, Ceib
|
|
1995
|
16 |
3S1 |
p. 122S-
1 p.
|
artikel
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| 180 |
P109 The role of a Regional Resource Center in a large multicenter clinical study
|
Margitić, Susan
|
|
1995
|
16 |
3S1 |
p. 134S-135S
nvt p.
|
artikel
|
| 181 |
P62 The role of the regional study coordinator in a multicenter clinical trial
|
Balanoff, Diane
|
|
1995
|
16 |
3S1 |
p. 108S-
1 p.
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artikel
|
| 182 |
P93 The value of pilot study data when designing randomized controlled trials for nonpharmacological interventions
|
Wilkins, Annette
|
|
1995
|
16 |
3S1 |
p. 125S-
1 p.
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artikel
|
| 183 |
P101 Time required for the protein intervention in the modification of diet in renal disease study
|
Olson, Marian
|
|
1995
|
16 |
3S1 |
p. 129S-130S
nvt p.
|
artikel
|
| 184 |
P02 Touchtone technologies: Let your fingers do the talking
|
Rushing, Scott
|
|
1995
|
16 |
3S1 |
p. 73S-74S
nvt p.
|
artikel
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| 185 |
P52 Tracing research subjects lost to follow-up with the aid of a National Credit Bureau
|
Vitek, Mary Ellen
|
|
1995
|
16 |
3S1 |
p. 102S-
1 p.
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artikel
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| 186 |
P20 (Un)predictability of monthly accrual in randomized clinical trials
|
Coates, Townes C.
|
|
1995
|
16 |
3S1 |
p. 83S-
1 p.
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artikel
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| 187 |
P77 Use of edit-query tables as a data management tool in clinical trials
|
Feak, Glen A.B.
|
|
1995
|
16 |
3S1 |
p. 116S-
1 p.
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artikel
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| 188 |
P89 Uses for large clinically accurate databases in clinical trial design
|
Crosby, Ann
|
|
1995
|
16 |
3S1 |
p. 123S-
1 p.
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artikel
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| 189 |
P118 Using cumulative plots to detect biased assignments in unbalanced designs
|
Helms, Laura E.
|
|
1995
|
16 |
3S1 |
p. 139S-
1 p.
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artikel
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| 190 |
P15 Using SAS© macros to automate data reports in multi-center clinical trials
|
Thompson, Chris
|
|
1995
|
16 |
3S1 |
p. 80S-81S
nvt p.
|
artikel
|
| 191 |
P50 Validity, reliability, and responsiveness of subjective self-assessment of symptoms in asthma clinical trials
|
Ih, Chang
|
|
1995
|
16 |
3S1 |
p. 101S-
1 p.
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artikel
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