| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A37 Accounting for missing data in clinical trials of blood pressure (BP) and hypertension
|
Cook, Nancy R.
|
|
1996
|
17 |
2S1 |
p. S59-S60
2 p.
|
artikel
|
| 2 |
A55 Adapting batch cleaning methods for lymphocyte data to on-line validation routines
|
Carrington, Jane
|
|
1996
|
17 |
2S1 |
p. S70-
1 p.
|
artikel
|
| 3 |
A08 A data manager training program for oncology clinical trials
|
Casagrande, Chris
|
|
1996
|
17 |
2S1 |
p. S42-
1 p.
|
artikel
|
| 4 |
A75 Adherence/compliance in a hormone replacement trial: The postmenopausal estrogen/progestins intervention (PEPI) trial perspective
|
Hogan, Patricia
|
|
1996
|
17 |
2S1 |
p. S82-
1 p.
|
artikel
|
| 5 |
A89 A dynamic approach to recruiting patients in a registry of coronary interventions
|
Holubkov, Richard
|
|
1996
|
17 |
2S1 |
p. S90-
1 p.
|
artikel
|
| 6 |
A74 A method to maintain blinding in a randomized trial requiring adjustment of doses for only one treatment arm
|
Mercier, Catherine
|
|
1996
|
17 |
2S1 |
p. S81-
1 p.
|
artikel
|
| 7 |
A23 analysis by intention to treat in randomized clinical trials: A survey of the literature
|
Jansen-McWilliams, Linda
|
|
1996
|
17 |
2S1 |
p. S51-
1 p.
|
artikel
|
| 8 |
A39 Analysis of agreement data beyond kappa: Application of loglinear modeling to evaluate agreement in disc photograph gradings
|
Hussein, M.E.
|
|
1996
|
17 |
2S1 |
p. S60-S61
2 p.
|
artikel
|
| 9 |
A40 Analytical issues for Stroke clinical trials
|
Tilley, Barbara C.
|
|
1996
|
17 |
2S1 |
p. S61-
1 p.
|
artikel
|
| 10 |
A59 An extension of stochastic curtailment for incompletely reported and classified data on recurrent outcomes: The multicenter study of hydroxyurea in sickle cell anemia (MSH)
|
McMahon, Robert P.
|
|
1996
|
17 |
2S1 |
p. S72-
1 p.
|
artikel
|
| 11 |
A70 An inexpensive electronic system for handling adverse event reports
|
Wong, Kenneth
|
|
1996
|
17 |
2S1 |
p. S79-
1 p.
|
artikel
|
| 12 |
A52 An interactive voice response system for randomizing patients
|
Assmann, Susan F.
|
|
1996
|
17 |
2S1 |
p. S68-S69
2 p.
|
artikel
|
| 13 |
A29 A program for large, simple randomized clinical trials — American style
|
Hillis, Argye
|
|
1996
|
17 |
2S1 |
p. S55-
1 p.
|
artikel
|
| 14 |
A49 Ascertainment of the primary end point in the multicenter study of hydroxyurea in sickle cell anemia (MSH)
|
Barton, F.
|
|
1996
|
17 |
2S1 |
p. S67-
1 p.
|
artikel
|
| 15 |
A72 Automatic forms processing with Windows 95: Hyperbole?
|
Wong, Kenneth
|
|
1996
|
17 |
2S1 |
p. S80-
1 p.
|
artikel
|
| 16 |
A34 Clinical monitoring of rating scales in multicenter clinical trials
|
Schafer, Kimberly
|
|
1996
|
17 |
2S1 |
p. S57-S58
2 p.
|
artikel
|
| 17 |
A35 Clinical trial Monitoring in the face of changing clinical practice
|
Thom, Elizabeth
|
|
1996
|
17 |
2S1 |
p. S58-S59
2 p.
|
artikel
|
| 18 |
A43 Collection of health care cost data in a VA health services study (CSHS#17)
|
Cramer, Joyce
|
|
1996
|
17 |
2S1 |
p. S63-
1 p.
|
artikel
|
| 19 |
A26 Combining parallel trials with differing eligibility criteria
|
Fowler, Sarah
|
|
1996
|
17 |
2S1 |
p. S52-S53
2 p.
|
artikel
|
| 20 |
A73 Comparability of self-report, pill count, and electronically monitored adherence data
|
Dunbar-Jacob, Jacqueline
|
|
1996
|
17 |
2S1 |
p. S80-S81
2 p.
|
artikel
|
| 21 |
A32 computer-aided clinical monitoring: Results of a controlled experiment
|
Thomas, Ronald G.
|
|
1996
|
17 |
2S1 |
p. S56-S57
2 p.
|
artikel
|
| 22 |
A03 Computing power in the design of clinical trials using ordered polychotomous logistic regression
|
Ernesto, Christopher
|
|
1996
|
17 |
2S1 |
p. S39-
1 p.
|
artikel
|
| 23 |
A20 Concurrent medication tracking in an oracle database in the African American Study of Kidney Disease and Hypertension
|
Stewart, Ron
|
|
1996
|
17 |
2S1 |
p. S49-
1 p.
|
artikel
|
| 24 |
A58 Consequences of data delay in a collaborative international sequentially monitored phase III prophylaxis trial
|
Hurwitz, Shelley
|
|
1996
|
17 |
2S1 |
p. S71-S72
2 p.
|
artikel
|
| 25 |
A71 Datafax and data quality in a large, multi-center, clinical trial
|
Krause-Steinrauf, Heidi
|
|
1996
|
17 |
2S1 |
p. S79-S80
2 p.
|
artikel
|
| 26 |
A80 Design of Phase II clinical trials incorporating response and early progression
|
Zee, Benny
|
|
1996
|
17 |
2S1 |
p. S85-
1 p.
|
artikel
|
| 27 |
A83 Design of the NIDCD/VA hearing aid trial
|
Henderson, William G.
|
|
1996
|
17 |
2S1 |
p. S86-S87
2 p.
|
artikel
|
| 28 |
A81 Diabetes prevention trial — type I (DPT-1) — design and implementation
|
Rafkin-Mervis, Lisa
|
|
1996
|
17 |
2S1 |
p. S85-S86
2 p.
|
artikel
|
| 29 |
A47 Differences in endpoint identification by investigators versus independent review
|
Tardiff, Barbara E.
|
|
1996
|
17 |
2S1 |
p. S65-S66
2 p.
|
artikel
|
| 30 |
A67 Double versus quadruple data entry
|
Maupas, Jean
|
|
1996
|
17 |
2S1 |
p. S77-
1 p.
|
artikel
|
| 31 |
A42 Economic evaluation alongside clinical trials: A problem or a solution?
|
Haider, Seema
|
|
1996
|
17 |
2S1 |
p. S62-
1 p.
|
artikel
|
| 32 |
A31 Ethical cost when the therapy target population and the dissemination population do not coincide
|
Boissel, Jean-Pierre
|
|
1996
|
17 |
2S1 |
p. S56-
1 p.
|
artikel
|
| 33 |
A02 Evaluation of phase I cancer clinical trial designs
|
Ahn, Chul
|
|
1996
|
17 |
2S1 |
p. S38-
1 p.
|
artikel
|
| 34 |
A09 Experience with interactive data management (IDM) in a Department of Veterans Affairs multi-center randomized clinical trial
|
Sacks, Jerome M.
|
|
1996
|
17 |
2S1 |
p. S42-S43
2 p.
|
artikel
|
| 35 |
A13 Exploring the information superhighway: Use of the internet in clinical drug trials
|
Carr, Sarah
|
|
1996
|
17 |
2S1 |
p. S44-S45
2 p.
|
artikel
|
| 36 |
A84 Extending intent-to-treat principles to cluster design clinical trials
|
Hirst, Kathryn
|
|
1996
|
17 |
2S1 |
p. S87-
1 p.
|
artikel
|
| 37 |
A36 Facilitating the quality assurance process of data collected during the research interview
|
Fischbach, Heidi E.
|
|
1996
|
17 |
2S1 |
p. S59-
1 p.
|
artikel
|
| 38 |
A69 Feasibility of keying data from screen-displayed facsimile images in the Collaborative Ocular Melanoma Study
|
Diener-West, Marie
|
|
1996
|
17 |
2S1 |
p. S78-
1 p.
|
artikel
|
| 39 |
A17 Format-independent data collection forms, the world-wide web, and reusable research data management: A proposal
|
Singer, Stephen W.
|
|
1996
|
17 |
2S1 |
p. S47-
1 p.
|
artikel
|
| 40 |
A21 graphical representation of symptom and concomitant treatment relationships
|
Visèle, Nathalie
|
|
1996
|
17 |
2S1 |
p. S49-S50
2 p.
|
artikel
|
| 41 |
A28 Impact of continuing education on general practitioners' behaviour: Methodological problems
|
Brun, Catherine
|
|
1996
|
17 |
2S1 |
p. S54-
1 p.
|
artikel
|
| 42 |
A30 Impact of the results of a trial on medical practice: Opinion survey among participating doctors
|
Blondel, Béatrice
|
|
1996
|
17 |
2S1 |
p. S55-
1 p.
|
artikel
|
| 43 |
A79 Innovative trial design solutions to problemsposed by a randomized,multinational, double-blindphase III study of cytomegalovirus prohylaxis in AIDS patients
|
Feinberg, Judith
|
|
1996
|
17 |
2S1 |
p. S84-
1 p.
|
artikel
|
| 44 |
A62 Issues in implementing a multi-centre, placebo controlled sequential design trialof anti-emetic prophylaxis (AEP)inpatients (pts) receiving radiotherapy (R)
|
Palmer, Michael J.
|
|
1996
|
17 |
2S1 |
p. S73-S74
2 p.
|
artikel
|
| 45 |
A78 Issues in monitoring adherence to protocol using timed urine collections: Methods for assessing the adequacy of urine samples
|
McFarlane, Mary
|
|
1996
|
17 |
2S1 |
p. S83-S84
2 p.
|
artikel
|
| 46 |
A24 Is the inclusion of the elderly in cancer and cardiovascular clinical trials increasing?
|
Davidson, Michael
|
|
1996
|
17 |
2S1 |
p. S51-S52
2 p.
|
artikel
|
| 47 |
A61 Likelihood analysis of sequential trials
|
Blume, Jeffrey
|
|
1996
|
17 |
2S1 |
p. S73-
1 p.
|
artikel
|
| 48 |
A50 Local versus central readings of endometrial biopsies in a multicenter clinical trial
|
Legault, Claudine
|
|
1996
|
17 |
2S1 |
p. S67-S68
2 p.
|
artikel
|
| 49 |
A63 Managing a blinded 9000-patient coumadin clinic using express mail and facsimile
|
Berdan, Lisa G.
|
|
1996
|
17 |
2S1 |
p. S74-
1 p.
|
artikel
|
| 50 |
A41 Methodological issues regarding variance estimation in cost evaluation
|
Ducruet, Thierry
|
|
1996
|
17 |
2S1 |
p. S61-S62
2 p.
|
artikel
|
| 51 |
A22 Methodological quality in randomized trials and statistical heterogeneity in meta-analyses
|
Schulz, Kenneth F.
|
|
1996
|
17 |
2S1 |
p. S50-S51
2 p.
|
artikel
|
| 52 |
A77 Modeling the association between compliance and response to treatment in primary prevention trials of cholesterol lowering drugs
|
Norrie, John
|
|
1996
|
17 |
2S1 |
p. S83-
1 p.
|
artikel
|
| 53 |
A64 Number of lines for telephone randomization
|
Kalish, Leslie A.
|
|
1996
|
17 |
2S1 |
p. S75-
1 p.
|
artikel
|
| 54 |
A46 Patient self-addressed postcard follow-up is inadequate: Results from the Duke Clinical Research Institute
|
Mahaffey, Kenneth W.
|
|
1996
|
17 |
2S1 |
p. S64-S65
2 p.
|
artikel
|
| 55 |
A66 Personnel certification and turnover in the collaborative ocular melanoma study
|
Church, Renée Y.
|
|
1996
|
17 |
2S1 |
p. S76-S77
2 p.
|
artikel
|
| 56 |
A15 Pilot-recruitment study for osteoporosis trial: Direct mailing versus GP-preselection
|
Bak, Annette
|
|
1996
|
17 |
2S1 |
p. S46-
1 p.
|
artikel
|
| 57 |
A86 Potential effects of slower than expected recruitment and proposed changes in eligibility criteria on power in a randomized controlled trial
|
Wright, Elizabeth C.
|
|
1996
|
17 |
2S1 |
p. S88-
1 p.
|
artikel
|
| 58 |
A65 Procedures for handling criticism and comments from study investigators
|
Gordon, Mae
|
|
1996
|
17 |
2S1 |
p. S76-
1 p.
|
artikel
|
| 59 |
A38 Proportional hazards model for assessing visual acuity data
|
Wisniewski, Stephen R.
|
|
1996
|
17 |
2S1 |
p. S60-
1 p.
|
artikel
|
| 60 |
A33 Quality management of a multicenter selective lymphadenectomy trial (MSLT): A model for success
|
Flaherty, Sandra
|
|
1996
|
17 |
2S1 |
p. S57-
1 p.
|
artikel
|
| 61 |
A88 Randomization to pharmacologic andbehavioral therapy separately within the same study and blinding issues
|
Cnaan, Avital
|
|
1996
|
17 |
2S1 |
p. S89-
1 p.
|
artikel
|
| 62 |
A14 Recruitment for a large-scale clinical study via the internet
|
Zadnik, K.
|
|
1996
|
17 |
2S1 |
p. S45-
1 p.
|
artikel
|
| 63 |
A16 Recruitment to breast cancer clinical trials
|
Morrill, Allison C.
|
|
1996
|
17 |
2S1 |
p. S46-S47
2 p.
|
artikel
|
| 64 |
A68 Results of rekey verification at the clinical centers in the hemodialysis (HEMO) study
|
Gassman, Jennifer
|
|
1996
|
17 |
2S1 |
p. S77-S78
2 p.
|
artikel
|
| 65 |
A48 Rigorous end point assessment procedures in reducing bias
|
Nelson, J.J.
|
|
1996
|
17 |
2S1 |
p. S66-
1 p.
|
artikel
|
| 66 |
A01 Samples sizes for phase II trials in multiple sclerosis
|
Schwid, Steven R.
|
|
1996
|
17 |
2S1 |
p. S38-
1 p.
|
artikel
|
| 67 |
A60 Stopping a clinical trial very early based on sequential conditional probability ratio test
|
Ming, Tan
|
|
1996
|
17 |
2S1 |
p. S72-S73
2 p.
|
artikel
|
| 68 |
A44 Strategies for including costs in randomized controlled trials of new medical technologies: The implementation of an economic analysis of an aicd (Automatic Implantable Cardiac Defibrillator)
|
Gajary, Elizabeth
|
|
1996
|
17 |
2S1 |
p. S63-S64
2 p.
|
artikel
|
| 69 |
A04 Survey of collaborators' opinions about study results
|
Weston, Julie
|
|
1996
|
17 |
2S1 |
p. S39-
1 p.
|
artikel
|
| 70 |
A27 Teaching the next generation of clinical trialists
|
Kelsey, Sheryl F.
|
|
1996
|
17 |
2S1 |
p. S53-S54
2 p.
|
artikel
|
| 71 |
A45 Team managed hospital based home care: Design of a multi-site randomized trial
|
Weaver, Frances
|
|
1996
|
17 |
2S1 |
p. S64-
1 p.
|
artikel
|
| 72 |
A18 Technical and architectural problems and solutions associated with registers of clinical trials
|
Strang, Nigel
|
|
1996
|
17 |
2S1 |
p. S48-
1 p.
|
artikel
|
| 73 |
A06 Termprom investigator survey
|
Hewson, Sheila
|
|
1996
|
17 |
2S1 |
p. S40-S41
2 p.
|
artikel
|
| 74 |
A76 The impact of method of calculation of electronically monitored adherence data
|
Rohay, Jeffrey M.
|
|
1996
|
17 |
2S1 |
p. S82-S83
2 p.
|
artikel
|
| 75 |
A87 The impact of using different albumin laboratory methods on eligibility in the HEMO study
|
Beck, Gerald
|
|
1996
|
17 |
2S1 |
p. S89-
1 p.
|
artikel
|
| 76 |
A82 The importance of the design of a pilot study providing the most exhaustive data for the protocol of a large controlled clinical trial
|
Gardinle, E.
|
|
1996
|
17 |
2S1 |
p. S86-
1 p.
|
artikel
|
| 77 |
A25 The prognostic profile of the patients is essential for any comparative interpretation of clinical trials
|
Hasford, J.
|
|
1996
|
17 |
2S1 |
p. S52-
1 p.
|
artikel
|
| 78 |
A56 Three gigabytes of transcranial doppler readings: Logistics of blinding the central readers and quality assurance in a 12 center clinical trial
|
Tighe, Foss
|
|
1996
|
17 |
2S1 |
p. S70-S71
2 p.
|
artikel
|
| 79 |
A85 Tools for the visualization of patient accrual trends in clinical trials
|
Buzydlowski, Jan W.
|
|
1996
|
17 |
2S1 |
p. S88-
1 p.
|
artikel
|
| 80 |
A19 Tracking monitoring activities performed at the Coordinating Center
|
Doherty, Irene
|
|
1996
|
17 |
2S1 |
p. S48-S49
2 p.
|
artikel
|
| 81 |
A07 Training and quality control procedures for remote database management of 24 hour dietary recalls
|
Doroshenko, Linda
|
|
1996
|
17 |
2S1 |
p. S41-
1 p.
|
artikel
|
| 82 |
A05 Treatment guesses by patients and investigators in a double-blind clinical trial
|
Barton, F.
|
|
1996
|
17 |
2S1 |
p. S40-
1 p.
|
artikel
|
| 83 |
A57 Use of a registry as control data: Data management issues in combining existing data into an existing registry
|
Kennard, Elizabeth D.
|
|
1996
|
17 |
2S1 |
p. S71-
1 p.
|
artikel
|
| 84 |
A53 Use of oracle with an interactive voice response system (IVR) to randomize patients in an acute controlled clinical trial
|
McPherson, Joseph A.
|
|
1996
|
17 |
2S1 |
p. S69-
1 p.
|
artikel
|
| 85 |
Author index
|
|
|
1996
|
17 |
2S1 |
p. S139-S154
16 p.
|
artikel
|
| 86 |
A51 Verification of endpoints in a phase 3 HIV clinical trial
|
Ingraham, Peter
|
|
1996
|
17 |
2S1 |
p. S68-
1 p.
|
artikel
|
| 87 |
A54 Window based data management system for clinical trials
|
Boardman, Chris
|
|
1996
|
17 |
2S1 |
p. S69-
1 p.
|
artikel
|
| 88 |
Calendar of program
|
|
|
1996
|
17 |
2S1 |
p. S3-S35
33 p.
|
artikel
|
| 89 |
Letter from the President
|
|
|
1996
|
17 |
2S1 |
p. S1-
1 p.
|
artikel
|
| 90 |
P45 Accessing data from external centralized sources to enhance analysis of a completed clinical trial
|
Abdellatif, Mazen
|
|
1996
|
17 |
2S1 |
p. S118-S119
2 p.
|
artikel
|
| 91 |
P59 A comparison of quantitative computerized and human panel coronary end point measures: Implications for angiographic trial design
|
Dunn, Meleana E.
|
|
1996
|
17 |
2S1 |
p. S128-
1 p.
|
artikel
|
| 92 |
P36 A comparison of statistical methodologies for the calculation of lytic units derived from the modeling of natural killer cells
|
Johnson, Paul
|
|
1996
|
17 |
2S1 |
p. S113-
1 p.
|
artikel
|
| 93 |
P07 A completely automated interactive data management system
|
Othman, Raslan
|
|
1996
|
17 |
2S1 |
p. S94-S95
2 p.
|
artikel
|
| 94 |
P05 Adapting management techniques after conversion to an onsite, interactive data management system (IDMS)
|
Ellis, Nancy
|
|
1996
|
17 |
2S1 |
p. S93-S94
2 p.
|
artikel
|
| 95 |
P64 Adverse medical events reported by patients in control groups
|
Raisch, Dennis W.
|
|
1996
|
17 |
2S1 |
p. S131-
1 p.
|
artikel
|
| 96 |
P37 A mixed models approach to the analysis of the treatment of delayed onset muscle soreness
|
Golloso-Nagpala, Fides R.
|
|
1996
|
17 |
2S1 |
p. S113-S114
2 p.
|
artikel
|
| 97 |
P53 An approximation of kappa's variance
|
Pintilie, Melania
|
|
1996
|
17 |
2S1 |
p. S124-S125
2 p.
|
artikel
|
| 98 |
P72 An iterative process for defining nonfatal endpoints in the context of clinical trials
|
Tardiff, Barbara E.
|
|
1996
|
17 |
2S1 |
p. S136-
1 p.
|
artikel
|
| 99 |
P33 Antidepressant evaluation: Methodological considerations for meta-analysis
|
Cialdella, Philippe
|
|
1996
|
17 |
2S1 |
p. S111-
1 p.
|
artikel
|
| 100 |
P09 A pilot study for feasibility of long-term patient follow-up after the end of a clinical trial
|
Beck, Gerald
|
|
1996
|
17 |
2S1 |
p. S95-S96
2 p.
|
artikel
|
| 101 |
P39 A quality control method for single-data entry using remote data entry systems in large compassionate clinical trials
|
Sharma, Inder J.
|
|
1996
|
17 |
2S1 |
p. S115-
1 p.
|
artikel
|
| 102 |
P15 Are specific trials needed to assess the best treatment duration? Examples in cardiovascular field
|
Gueyffier, François
|
|
1996
|
17 |
2S1 |
p. S99-S100
2 p.
|
artikel
|
| 103 |
P32 A SAS macro for exploratory data analysis using a Bayesian Belief Network
|
Clarke, Ellis
|
|
1996
|
17 |
2S1 |
p. S110-
1 p.
|
artikel
|
| 104 |
P56 Assessment and reorganization of educational training programs developed for data managers
|
Edelman, Bonnie
|
|
1996
|
17 |
2S1 |
p. S126-
1 p.
|
artikel
|
| 105 |
P48 Auditing and verification of clinical data: A coordinating center's role
|
Randall, A.M.Y.
|
|
1996
|
17 |
2S1 |
p. S121-
1 p.
|
artikel
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| 106 |
P06 Automated edit system from data entry to site notification
|
Harrison, Merrie Jean
|
|
1996
|
17 |
2S1 |
p. S94-
1 p.
|
artikel
|
| 107 |
P52 Can the forest plot be simplified without loosing relevant information in meta-analyses?
|
Bijnens, Luc
|
|
1996
|
17 |
2S1 |
p. S124-
1 p.
|
artikel
|
| 108 |
P30 Challenges in recruiting normal volunteers for clinical trials
|
Herr, Barbara
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|
1996
|
17 |
2S1 |
p. S109-
1 p.
|
artikel
|
| 109 |
P49 Combining graphical and tabular displays in data monitoring reports
|
Van Natta, Mark L.
|
|
1996
|
17 |
2S1 |
p. S121-S122
2 p.
|
artikel
|
| 110 |
P46 Comparability of absolute/percent CD4+ T-lymphocytes completed locally and centrally
|
Donfield, Sharyne
|
|
1996
|
17 |
2S1 |
p. S119-
1 p.
|
artikel
|
| 111 |
P73 Comparison of investigator and central events review of myocardial infarction rates as a means to improve events classification: Results from GUSTO-IIa
|
Mahaffey, Kenneth W.
|
|
1996
|
17 |
2S1 |
p. S136-S137
2 p.
|
artikel
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| 112 |
P51 Concordance of medication adherence measures in primary Raynaud's disease
|
Schlenk, Elizabeth A.
|
|
1996
|
17 |
2S1 |
p. S123-
1 p.
|
artikel
|
| 113 |
P04 Consistency checks in a multi-centered clinical study
|
Konig, Victoria
|
|
1996
|
17 |
2S1 |
p. S93-
1 p.
|
artikel
|
| 114 |
P47 Data management for a Phase III international collaborative study (AIDS clinical trial group study 204/Glaxo Wellcome protocol 123-014)
|
Fry, J.
|
|
1996
|
17 |
2S1 |
p. S120-
1 p.
|
artikel
|
| 115 |
P69 Does workspace effect coordinator performance in a randomized clinical trial?
|
Manos, Kelly S.
|
|
1996
|
17 |
2S1 |
p. S134-
1 p.
|
artikel
|
| 116 |
P03 Dose titration in the multicenter study of hydroxyurea in sickle cell anemia (MSH)
|
Handy, C.
|
|
1996
|
17 |
2S1 |
p. S92-
1 p.
|
artikel
|
| 117 |
P54 Drug packaging challenges in a multicenter trial on opiate dependence
|
Johnson, Elaine L.
|
|
1996
|
17 |
2S1 |
p. S125-
1 p.
|
artikel
|
| 118 |
P08 Edit check: An easy way to clean clinical studies databases
|
Charpentier, B.
|
|
1996
|
17 |
2S1 |
p. S95-
1 p.
|
artikel
|
| 119 |
P12 Efforts to assess subject participation
|
Clerici, Annette M.
|
|
1996
|
17 |
2S1 |
p. S97-S98
2 p.
|
artikel
|
| 120 |
P13 Efforts to enhance participation in a low socio-economic status population
|
Clerici, Annette M.
|
|
1996
|
17 |
2S1 |
p. S98-
1 p.
|
artikel
|
| 121 |
P28 How to achieve successful site participation in a large simple trial
|
Egan, Debra
|
|
1996
|
17 |
2S1 |
p. S108-
1 p.
|
artikel
|
| 122 |
P71 Impact of the clinical events committee process on data safety monitoring
|
Tardiff, Barbara E.
|
|
1996
|
17 |
2S1 |
p. S135-
1 p.
|
artikel
|
| 123 |
P63 Informed consent issues when including genetic testing in clinical trials
|
Schafer, Kimberly
|
|
1996
|
17 |
2S1 |
p. S130-S131
2 p.
|
artikel
|
| 124 |
P58 Intention to treat analysis and the need for supplemental approaches for some trial designs
|
Panzarella, Tony
|
|
1996
|
17 |
2S1 |
p. S127-S128
2 p.
|
artikel
|
| 125 |
P42 Logistics of interim mortality ascertainment
|
Crow, Sharon W.
|
|
1996
|
17 |
2S1 |
p. S116-S117
2 p.
|
artikel
|
| 126 |
P57 Longitudinal variability of ultrasonographic measurements of carotid intimal-medial thickness: Results for ACAPS
|
Craven, Timothy
|
|
1996
|
17 |
2S1 |
p. S127-
1 p.
|
artikel
|
| 127 |
P35 Methodological issues in evaluating graft materials for lumbar spinal fusion
|
Block, Jon E.
|
|
1996
|
17 |
2S1 |
p. S112-
1 p.
|
artikel
|
| 128 |
P50 Minimization technologies in randomized open intervention studies
|
Weverling, Gerrit J.
|
|
1996
|
17 |
2S1 |
p. S122-S123
2 p.
|
artikel
|
| 129 |
P26 Monitoring in a large multicentre international clinical trial: The italian experience in core study
|
Bonfanti, E.
|
|
1996
|
17 |
2S1 |
p. S106-S107
2 p.
|
artikel
|
| 130 |
P11 Monitoring item bias within the SF-36: A bias toward decreased health perception
|
Wasser, Thomas
|
|
1996
|
17 |
2S1 |
p. S97-
1 p.
|
artikel
|
| 131 |
P17 Multicenter trials and cohort studies — valuable resources for long term studies of disease outcomes
|
Wright, Elizabeth
|
|
1996
|
17 |
2S1 |
p. S101-
1 p.
|
artikel
|
| 132 |
P62 On-site monitoring of a multicenter clinical trial: Perspectives from the administrative center, data coordinating center, clinical centers, auditors. And the funding agency
|
Howard, Virginia J.
|
|
1996
|
17 |
2S1 |
p. S130-
1 p.
|
artikel
|
| 133 |
P14 Outcomes of a placebo run-in period in a cancer chemoprevention trial
|
Hudmon, Karen Suchanek
|
|
1996
|
17 |
2S1 |
p. S99-
1 p.
|
artikel
|
| 134 |
P20 Participant perception of the role and benefits of study coordinators: Results of a pilot study
|
Mitchell, Jayne
|
|
1996
|
17 |
2S1 |
p. S103-
1 p.
|
artikel
|
| 135 |
P27 Predictors of missed follow-up interviews in a study of asthma among inner-city children
|
Islam, Shaheen U.
|
|
1996
|
17 |
2S1 |
p. S107-
1 p.
|
artikel
|
| 136 |
P68 Primary outcome verification in a multicenter clinical trial
|
Das, Anita
|
|
1996
|
17 |
2S1 |
p. S133-S134
2 p.
|
artikel
|
| 137 |
P29 Prognostic significance of cardiac enzyme elevations detected through systematic screening in clinical trials
|
Tardiff, Barbara E.
|
|
1996
|
17 |
2S1 |
p. S108-S109
2 p.
|
artikel
|
| 138 |
P34 Proposed strategy for identifying the treatment target population
|
Gueyffier, François
|
|
1996
|
17 |
2S1 |
p. S111-S112
2 p.
|
artikel
|
| 139 |
P18 Prospective case-control studies,following a large multicentre clinical trial: GISSI-2
|
Bonfanti, E.
|
|
1996
|
17 |
2S1 |
p. S101-S102
2 p.
|
artikel
|
| 140 |
P43 Quality assurance in a multicenter/multidisciplinary clinical trial — A model for a limited budget
|
Stern, Stacey
|
|
1996
|
17 |
2S1 |
p. S117-
1 p.
|
artikel
|
| 141 |
P74 Quality of life (QL) as an outcome measure in the assessment of nausea (N) and vomiting (V)
|
Pater, J.L.
|
|
1996
|
17 |
2S1 |
p. S137-
1 p.
|
artikel
|
| 142 |
P01 Randomization systems in an international multicentre clinical trial: The CORE study
|
Santoro, E.
|
|
1996
|
17 |
2S1 |
p. S91-
1 p.
|
artikel
|
| 143 |
P22 Randomized and non-randomized patients in large clinical trials: The case of GISSI
|
Franzosi, M.G.
|
|
1996
|
17 |
2S1 |
p. S104-
1 p.
|
artikel
|
| 144 |
P70 Recruitment of study sites for participation in a proposed clinical trial
|
Hewson, Sheila
|
|
1996
|
17 |
2S1 |
p. S135-
1 p.
|
artikel
|
| 145 |
P02 Reducing variations in care in the acute myocardial infarction (AMI) patient using medical practice guidelines
|
Reed III, James F.
|
|
1996
|
17 |
2S1 |
p. S91-S92
2 p.
|
artikel
|
| 146 |
P31 Reliability of economic and quality of life data for collection of follow-up clinical outcome information
|
Tardiff, Barbara E.
|
|
1996
|
17 |
2S1 |
p. S110-
1 p.
|
artikel
|
| 147 |
P25 Representativeness of clinical trial participants: The hemodialysis study
|
Kusek, John W.
|
|
1996
|
17 |
2S1 |
p. S106-
1 p.
|
artikel
|
| 148 |
P67 Social factors influence dietary satisfaction in the modification of diet in renal disease study
|
Olson, Marian
|
|
1996
|
17 |
2S1 |
p. S133-
1 p.
|
artikel
|
| 149 |
P60 Standardizing data collection by interviewers on a multi-site longitudinal research study
|
Fischbach, Heidi E.
|
|
1996
|
17 |
2S1 |
p. S128-S129
2 p.
|
artikel
|
| 150 |
P21 Steps in the development of a disease-specific quality of life measure
|
Fink, Nancy
|
|
1996
|
17 |
2S1 |
p. S103-S104
2 p.
|
artikel
|
| 151 |
P38 System for monitoring timing of data review and entry: A tool for internal data quality control
|
Zee, Benny
|
|
1996
|
17 |
2S1 |
p. S114-
1 p.
|
artikel
|
| 152 |
P16 Tailoring interventions for children in the inner-city
|
Mitchell, Herman E.
|
|
1996
|
17 |
2S1 |
p. S100-S101
2 p.
|
artikel
|
| 153 |
P61 The application of pharmacokinetic modeling to the predication of drug needs during multicenter clinical trials
|
Barnhill, Jamie G.
|
|
1996
|
17 |
2S1 |
p. S129-
1 p.
|
artikel
|
| 154 |
P40 The design of a windows-based cati software system
|
Goldstein, Robert B.
|
|
1996
|
17 |
2S1 |
p. S115-S116
2 p.
|
artikel
|
| 155 |
P10 The efficacy of testosterone treatment in HIV-related wasting: Does testosteronereplacement help?
|
Cofrancesco Jr., Joseph
|
|
1996
|
17 |
2S1 |
p. S96-
1 p.
|
artikel
|
| 156 |
P65 The impact of early closure of a clinical trial on a related study
|
Cloud, Gretchen
|
|
1996
|
17 |
2S1 |
p. S131-S132
2 p.
|
artikel
|
| 157 |
P23 The role of a regional data coordinating centre (RDCC) in a multi-national large phase-II trial
|
Franzosi, M.G.
|
|
1996
|
17 |
2S1 |
p. S104-S105
2 p.
|
artikel
|
| 158 |
P55 Treatment discontinuation in a Phase III cytomegalovirus prophylaxis trial: Design and analysis
|
Hurwitz, Shelley
|
|
1996
|
17 |
2S1 |
p. S125-S126
2 p.
|
artikel
|
| 159 |
P24 Tunnel vision: A flaw to avoid when preparing study materials
|
Liu, Margaret B.
|
|
1996
|
17 |
2S1 |
p. S105-
1 p.
|
artikel
|
| 160 |
P44 Using SAS and wordperfect to automate the production of study data tables
|
Horney, R.Anne
|
|
1996
|
17 |
2S1 |
p. S118-
1 p.
|
artikel
|
| 161 |
P66 Variables associated with successful site performance in a large, randomized, chronic heart failure trial
|
Rendall, David
|
|
1996
|
17 |
2S1 |
p. S132-
1 p.
|
artikel
|
| 162 |
P41 Weeding out bad apples: Monitoring data quality in RCTs
|
Flann, M.A.
|
|
1996
|
17 |
2S1 |
p. S116-
1 p.
|
artikel
|
| 163 |
P19 Why do patients accept or decline randomization?
|
Rajab, Mohammad Hasan
|
|
1996
|
17 |
2S1 |
p. S102-
1 p.
|
artikel
|
| 164 |
S11 Internal estimation of the sample size for a t-test
|
Denne, Jonathan S.
|
|
1996
|
17 |
2S1 |
p. S43-
1 p.
|
artikel
|
| 165 |
S10 Planning clinical trials to evaluate early detection programs
|
Hu, Ping
|
|
1996
|
17 |
2S1 |
p. S43-
1 p.
|
artikel
|
| 166 |
S12 Standardized computer-based reporting of clinical trials: In support of meta-analysis
|
Sim, Ida
|
|
1996
|
17 |
2S1 |
p. S44-
1 p.
|
artikel
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