| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A coding system for medication use based on the American hospital formulary service
|
Pierce, J.
|
|
1992
|
13 |
5 |
p. 436-
1 p.
|
artikel
|
| 2 |
A comparison of statistical methods of pooling randomized control trials (RCTs): An assessment of 45 + meta-analyses (M-As)
|
Lau, Joseph
|
|
1992
|
13 |
5 |
p. 422-
1 p.
|
artikel
|
| 3 |
A comparison of three database packages—SIR, Paradox, and DbaseIV— with respect to their ability to perform data management tasks
|
Weston, Julie A.
|
|
1992
|
13 |
5 |
p. 434-
1 p.
|
artikel
|
| 4 |
A controlled clinical trial in ophthalmology: Formal randomization may not be ethical
|
Ballantyne, Margaret
|
|
1992
|
13 |
5 |
p. 412-
1 p.
|
artikel
|
| 5 |
A deming approach to recruiting: The National Institute of Neurological disorders and stroke (NINDS) t-PA stroke trial experience
|
Tilley, Barbara
|
|
1992
|
13 |
5 |
p. 428-429
2 p.
|
artikel
|
| 6 |
Advantages and limitations of meta-analytic regressions of clinical trials data
|
Berlin, Jesse A.
|
|
1992
|
13 |
5 |
p. 422-
1 p.
|
artikel
|
| 7 |
Adverse medical events in clinical trials: Reporting and evaluation
|
Day, Philip
|
|
1992
|
13 |
5 |
p. 384-
1 p.
|
artikel
|
| 8 |
A likelihood-based graphical method for meta-analysis
|
Goodman, Steven N.
|
|
1992
|
13 |
5 |
p. 377-378
2 p.
|
artikel
|
| 9 |
A low cost screening survey to assess sample yield and refine study entry criteria
|
Gordon, Mae O.
|
|
1992
|
13 |
5 |
p. 392-393
2 p.
|
artikel
|
| 10 |
An ABC of information management in primary prevention trials
|
Duncan, David
|
|
1992
|
13 |
5 |
p. 399-
1 p.
|
artikel
|
| 11 |
Analysis of risk factors for conditions defined by extremes of a distribution
|
Barton, Bruce
|
|
1992
|
13 |
5 |
p. 440-
1 p.
|
artikel
|
| 12 |
An application of an extended Greco-Latin square design to study gender and race bias
|
Marcus, Sue M.
|
|
1992
|
13 |
5 |
p. 411-
1 p.
|
artikel
|
| 13 |
An illustrative statistical analysis of cutoff-based randomized clinical trials
|
Cappelleri, Joseph C.
|
|
1992
|
13 |
5 |
p. 378-
1 p.
|
artikel
|
| 14 |
An inventoried editing system: Efficient maintenance of high standards in data quality
|
Lawlor, Sharon
|
|
1992
|
13 |
5 |
p. 417-
1 p.
|
artikel
|
| 15 |
A phase II elimination procedure of treatments for a serious illness
|
Palmer, Christopher R.
|
|
1992
|
13 |
5 |
p. 387-
1 p.
|
artikel
|
| 16 |
A predictive model of inclusion rates in a very large scale clinical trial with general practitioners
|
Alamercery, Y.
|
|
1992
|
13 |
5 |
p. 428-
1 p.
|
artikel
|
| 17 |
A questionnaire to measure morbidity in patients receiving radiation therapy for head and neck cancer
|
Skingley, Peter
|
|
1992
|
13 |
5 |
p. 389-
1 p.
|
artikel
|
| 18 |
Are habitual volunteers a problem in clinical trials?
|
Morris, Mary
|
|
1992
|
13 |
5 |
p. 392-
1 p.
|
artikel
|
| 19 |
Are science and seeding “trials” compatible?
|
Boissel, Jean-Pierre
|
|
1992
|
13 |
5 |
p. 409-
1 p.
|
artikel
|
| 20 |
Are there gender-related differences among attitudes of patients in heart failure trials?
|
Blackburn, Glenda H.
|
|
1992
|
13 |
5 |
p. 432-
1 p.
|
artikel
|
| 21 |
ARGO: An on-line drug prescription monitoring system
|
DeRosa, M.
|
|
1992
|
13 |
5 |
p. 385-386
2 p.
|
artikel
|
| 22 |
A sample size formula for case-control studies with an independent variable that is continuous
|
Thompson, Bruce
|
|
1992
|
13 |
5 |
p. 413-414
2 p.
|
artikel
|
| 23 |
A software for registration and stratified randomization in multicenter clinical trials: The experience of the European lung cancer working party
|
Paesmans, M.
|
|
1992
|
13 |
5 |
p. 430-
1 p.
|
artikel
|
| 24 |
Assessing disease-specific causes of death in a trial of all-cause mortality
|
Markowitz, Jan A.
|
|
1992
|
13 |
5 |
p. 389-
1 p.
|
artikel
|
| 25 |
Assessing patient satisfaction in randomized clinical trials: Some design measurement issues
|
Moher, David
|
|
1992
|
13 |
5 |
p. 397-
1 p.
|
artikel
|
| 26 |
Assessing quality of life in clinical trials
|
Hoop, R.S.
|
|
1992
|
13 |
5 |
p. 413-
1 p.
|
artikel
|
| 27 |
Bar coding in validating investigational drug packaging
|
Jones, Mark S.
|
|
1992
|
13 |
5 |
p. 384-385
2 p.
|
artikel
|
| 28 |
Bayesian decision-theoretic clinical trials: Monte Carlo comparison with classical group sequential methods
|
Lewis, Roger J.
|
|
1992
|
13 |
5 |
p. 414-415
2 p.
|
artikel
|
| 29 |
Bayesian guidelines for phase II clinical trial design and analysis
|
Thall, Peter F.
|
|
1992
|
13 |
5 |
p. 377-
1 p.
|
artikel
|
| 30 |
Blocked randomized assignment of treatments to patients in clinical trials using SAS(Statistical Analysis System)
|
Deloria, Maria A.
|
|
1992
|
13 |
5 |
p. 410-
1 p.
|
artikel
|
| 31 |
Cast coordinator survey
|
Kellen, Joyce C.
|
|
1992
|
13 |
5 |
p. 404-405
2 p.
|
artikel
|
| 32 |
Chiropractic and pharmaceutical treatment for muscle tension headaches: A randomized clinical trial
|
Boline, Patrick D.
|
|
1992
|
13 |
5 |
p. 407-408
2 p.
|
artikel
|
| 33 |
Classification of protocol deviations in a complex study
|
Moy, Claudia S.
|
|
1992
|
13 |
5 |
p. 390-391
2 p.
|
artikel
|
| 34 |
Clinical trial enrollers versus nonenrollers: Recruitment and enrollment assessment in clinical trials (react) project
|
Gorkin, Larry
|
|
1992
|
13 |
5 |
p. 423-
1 p.
|
artikel
|
| 35 |
Clinical trials of informed consent
|
Simel, David L.
|
|
1992
|
13 |
5 |
p. 321-324
4 p.
|
artikel
|
| 36 |
Clinical use of logistic regression models to predict treatment efficacy in the presence of treatment-covariate interaction
|
Moritz, Thomas E.
|
|
1992
|
13 |
5 |
p. 382-
1 p.
|
artikel
|
| 37 |
Collaboration between universities and the pharmaceutical industry—A European perspective
|
|
|
1992
|
13 |
5 |
p. 406-
1 p.
|
artikel
|
| 38 |
Common toxicity criteria: The National Cancer Institute of Canada Clinical Trials Group (NCIC CTG) experience
|
Wainman, Nancy
|
|
1992
|
13 |
5 |
p. 435-
1 p.
|
artikel
|
| 39 |
Comparing trials for the treatment of myelomatosis
|
Dunn, Janet A.
|
|
1992
|
13 |
5 |
p. 441-
1 p.
|
artikel
|
| 40 |
Comparison between two drug titration systems developed for the post-CABG studies clinical trial
|
Mirenzi, Evelyn
|
|
1992
|
13 |
5 |
p. 437-
1 p.
|
artikel
|
| 41 |
Comparison of two methods of classification of cause of death in a cardiovascular clinical trial
|
Feldman, George
|
|
1992
|
13 |
5 |
p. 399-
1 p.
|
artikel
|
| 42 |
Computer-assisted clinic monitoring: The COMS experience
|
Manos, Kelly S.
|
|
1992
|
13 |
5 |
p. 416-
1 p.
|
artikel
|
| 43 |
Computer-assisted eligibility review and randomization
|
Newhouse, M.Marvin
|
|
1992
|
13 |
5 |
p. 400-
1 p.
|
artikel
|
| 44 |
Computer generated drug distribution and accountability for a clinical trial
|
McGrath, P.D.
|
|
1992
|
13 |
5 |
p. 439-
1 p.
|
artikel
|
| 45 |
Computer models for editing study data
|
Karabelas, Susan
|
|
1992
|
13 |
5 |
p. 415-
1 p.
|
artikel
|
| 46 |
Conducting clinical trials with database controls
|
Murphy, James R.
|
|
1992
|
13 |
5 |
p. 412-
1 p.
|
artikel
|
| 47 |
Confidence intervals for the difference of two survival probabilities: A comparative study
|
Gupta, Sudhir
|
|
1992
|
13 |
5 |
p. 419-
1 p.
|
artikel
|
| 48 |
Congestive heart failure: Survival trial of antiarrhythmic therapy (CHF STAT)
|
Singh, Steven
|
|
1992
|
13 |
5 |
p. 339-350
12 p.
|
artikel
|
| 49 |
Continuing review of trials by local ethics boards: A reminder system for keeping participating centres on track
|
Paul, Nancy
|
|
1992
|
13 |
5 |
p. 431-
1 p.
|
artikel
|
| 50 |
Conventions for handling missing data
|
Ward, Linda
|
|
1992
|
13 |
5 |
p. 440-
1 p.
|
artikel
|
| 51 |
Cooperative clinical trials in health services research in the department of veterans affairs
|
Henderson, William G.
|
|
1992
|
13 |
5 |
p. 409-
1 p.
|
artikel
|
| 52 |
Cost utility analysis of maintenance treatment for recurrent depression
|
Paul, Nancy
|
|
1992
|
13 |
5 |
p. 381-
1 p.
|
artikel
|
| 53 |
Cox regression analyses using SAS/PHREG
|
Donithan, Michele
|
|
1992
|
13 |
5 |
p. 420-
1 p.
|
artikel
|
| 54 |
Crisis management: A coordinating center's experience with the suspension of a aids treatment protocol for a clinical trial
|
Holbrook, Janet T.
|
|
1992
|
13 |
5 |
p. 394-
1 p.
|
artikel
|
| 55 |
Databases-a relational design the pros and cons
|
Wainwright, Paul
|
|
1992
|
13 |
5 |
p. 418-
1 p.
|
artikel
|
| 56 |
Data collection forms in clinical trials
|
de Pauw, M.
|
|
1992
|
13 |
5 |
p. 351-352
2 p.
|
artikel
|
| 57 |
Data entry manual for a clinical trial
|
Corely, Scott
|
|
1992
|
13 |
5 |
p. 417-
1 p.
|
artikel
|
| 58 |
Design and implementation of the NHLBI and the VA cooperative studies program collaborative study, “trial to evaluate the effect of digitalis on motality in heart failure”
|
Williford, William O.
|
|
1992
|
13 |
5 |
p. 386-
1 p.
|
artikel
|
| 59 |
Design issues for studies based on ultrasonographic measurement of the carotid artery intimal-medial thickness
|
Espeland, Mark A.
|
|
1992
|
13 |
5 |
p. 379-
1 p.
|
artikel
|
| 60 |
Design of the veterans administration cooperative study of active immunotherapy of HIV infection
|
Peduzzi, Peter
|
|
1992
|
13 |
5 |
p. 386-
1 p.
|
artikel
|
| 61 |
Determinants of clinical center staff size: Ophthalmologists and ophthalmic photographers certified in a large multi-center trial
|
|
|
1992
|
13 |
5 |
p. 405-
1 p.
|
artikel
|
| 62 |
Developing a prognostic index for stomach cancer
|
Dunn, Janet A.
|
|
1992
|
13 |
5 |
p. 427-
1 p.
|
artikel
|
| 63 |
Developing clinical trial quality management principles
|
Barker, Christopher
|
|
1992
|
13 |
5 |
p. 395-
1 p.
|
artikel
|
| 64 |
Development of a composite index for noncompliance patients in clinical trials
|
De Rosa, M.
|
|
1992
|
13 |
5 |
p. 436-
1 p.
|
artikel
|
| 65 |
Development of a computerized 24-hour-a-day randomization service
|
Weston, Julie A.
|
|
1992
|
13 |
5 |
p. 401-402
2 p.
|
artikel
|
| 66 |
Documentation and analysis of adverse event data in clinical trials: The German chronic myeloid leukemia study experience
|
Hasford, Joerg
|
|
1992
|
13 |
5 |
p. 442-
1 p.
|
artikel
|
| 67 |
Effect of selective decontamination of the digestive tract (SSD) upon mortality
|
Brazzi, Luca
|
|
1992
|
13 |
5 |
p. 391-
1 p.
|
artikel
|
| 68 |
Eligible-non-randomized patients: Their impact on generalizability
|
Marcellus, Deborah
|
|
1992
|
13 |
5 |
p. 391-
1 p.
|
artikel
|
| 69 |
Estimating sensitivity, specificity and prevalence from clinical trials of multiple screening tests
|
Church, Timothy R.
|
|
1992
|
13 |
5 |
p. 398-
1 p.
|
artikel
|
| 70 |
Estimation in clinical trials that stop early
|
Brooks, Maria Mori
|
|
1992
|
13 |
5 |
p. 379-380
2 p.
|
artikel
|
| 71 |
Evaluation of coronary arteriography changes as a surrogate endpoint for atherosclerotic cardiac events
|
Matts, John P.
|
|
1992
|
13 |
5 |
p. 379-
1 p.
|
artikel
|
| 72 |
Evaluation of the impact of legal regulations on the quality of trials in Spain
|
Garcia-Lopez, Fernando
|
|
1992
|
13 |
5 |
p. 407-
1 p.
|
artikel
|
| 73 |
Facilitating investigator recruitment
|
Halloran, Laurie A.
|
|
1992
|
13 |
5 |
p. 405-406
2 p.
|
artikel
|
| 74 |
Features of manuals of procedures for multicenter randomized clinical trials
|
Moy, Claudia S.
|
|
1992
|
13 |
5 |
p. 403-
1 p.
|
artikel
|
| 75 |
Fiscal administration of clinics by coordinating centers: A survey of multicenter eye trials
|
Gerczak, Charlotte
|
|
1992
|
13 |
5 |
p. 406-
1 p.
|
artikel
|
| 76 |
Form enhances content: Development of a generic protocol (GP)
|
Paul, Nancy
|
|
1992
|
13 |
5 |
p. 395-
1 p.
|
artikel
|
| 77 |
Fouteenth annual meeting the society for clinical trials May 23–26, 1993 Hilton Hotel Orlando, Florida
|
|
|
1992
|
13 |
5 |
p. 353-
1 p.
|
artikel
|
| 78 |
Graphical display of Kaplan-Meier plots
|
Van Natta, Mark
|
|
1992
|
13 |
5 |
p. 419-420
2 p.
|
artikel
|
| 79 |
Graphical methods for visualizing the timing of follow-up in clinical studies
|
Lesser, Martin L.
|
|
1992
|
13 |
5 |
p. 419-
1 p.
|
artikel
|
| 80 |
Health care directives in the elderly and health care utilization
|
Molloy, D.W.
|
|
1992
|
13 |
5 |
p. 432-
1 p.
|
artikel
|
| 81 |
Impact of a randomized trial on transfusion practice in orthopedic surgery
|
Dickson, Lenore
|
|
1992
|
13 |
5 |
p. 431-
1 p.
|
artikel
|
| 82 |
Improving the classification of stage: A potential problem for comparative studies
|
Ward, Linda
|
|
1992
|
13 |
5 |
p. 390-
1 p.
|
artikel
|
| 83 |
Lessons for coordinating center management from a centralized, computer-assisted randomization system
|
Coates, Townes C.
|
|
1992
|
13 |
5 |
p. 429-
1 p.
|
artikel
|
| 84 |
Lessons learned and pitfalls to be avoided in the design of study drug titration systems
|
Fox, Norma Lynn
|
|
1992
|
13 |
5 |
p. 384-
1 p.
|
artikel
|
| 85 |
Long term adherence in patients who fail the initial prerandomization adherence screen: The studies of left ventricular dysfunction experience
|
Henzlova, Milena
|
|
1992
|
13 |
5 |
p. 425-
1 p.
|
artikel
|
| 86 |
Low dose oral anticoagulation and cardiac valvular replacement: Application of the eligibility oriented randomization scheme
|
Bossard, Nadine
|
|
1992
|
13 |
5 |
p. 411-
1 p.
|
artikel
|
| 87 |
Mean daytime diastolic blood pressure as an entry criterion in a parallel factorial design study to assess the antihypertensive efficacy of nebivolol alone or in combination with hydrochlorothiazide
|
Lefebvre, J.
|
|
1992
|
13 |
5 |
p. 387-
1 p.
|
artikel
|
| 88 |
Meta-analysis of randomized controlled trials of the benefits of screening women ages 40–49
|
Chu, Kenneth C.
|
|
1992
|
13 |
5 |
p. 423-
1 p.
|
artikel
|
| 89 |
Meta-analysis or quantitative overview: Is there any difference?
|
Stewart, Lesley A.
|
|
1992
|
13 |
5 |
p. 422-423
2 p.
|
artikel
|
| 90 |
Methodological and ethical issues in a series of exploratory multiple crossover double-blind studies in individual patients with dementia to assess the efficacy and safety of CGS 5649B
|
Molloy, D.W.
|
|
1992
|
13 |
5 |
p. 410-411
2 p.
|
artikel
|
| 91 |
Methodological issues in screening for relapse in early breast cancer
|
Fossati, Roldano
|
|
1992
|
13 |
5 |
p. 426-
1 p.
|
artikel
|
| 92 |
Modelling the time-varying course of compliance in a clinical trial
|
Glynn, Robert J.
|
|
1992
|
13 |
5 |
p. 382-
1 p.
|
artikel
|
| 93 |
Monitoring investigator compliance
|
Odom-Maryon, Tamara
|
|
1992
|
13 |
5 |
p. 404-
1 p.
|
artikel
|
| 94 |
Multistage screening for a lipid-restricted population: The VA HDL intervention trial (HIT)
|
Iwane, Marika
|
|
1992
|
13 |
5 |
p. 393-394
2 p.
|
artikel
|
| 95 |
Multistage screening for entry into clinical trials
|
Wittes, Janet
|
|
1992
|
13 |
5 |
p. 393-
1 p.
|
artikel
|
| 96 |
NHLBI growth and health study remote clinical data systems: 5 years later
|
Clarke, Ellis J.
|
|
1992
|
13 |
5 |
p. 417-
1 p.
|
artikel
|
| 97 |
Nonparametric survival regression trees and application to three radiation therapy oncology group (RTOG) malignant glioma trials
|
Scott, Charles B.
|
|
1992
|
13 |
5 |
p. 383-
1 p.
|
artikel
|
| 98 |
Non-ulcer dyspepsia and the randomized multiple cross-over model
|
Höschen, K.
|
|
1992
|
13 |
5 |
p. 424-
1 p.
|
artikel
|
| 99 |
Observational analyses with time dependency and missing values in the thrombolysis in myocardial infarction (TIMI) II clinical trial
|
Terrin, Michael L.
|
|
1992
|
13 |
5 |
p. 383-
1 p.
|
artikel
|
| 100 |
Officers—Board of directors 1992–1993
|
|
|
1992
|
13 |
5 |
p. 354-
1 p.
|
artikel
|
| 101 |
One-sided test for clinical trials with group sequential design that allow early acceptance of negative result
|
Zee, Benny C.
|
|
1992
|
13 |
5 |
p. 380-
1 p.
|
artikel
|
| 102 |
Online with WHO: Electronic medication coding
|
Gallinger, Kathleen
|
|
1992
|
13 |
5 |
p. 437-
1 p.
|
artikel
|
| 103 |
Organization, goals, and logistical challenges of the community programs for clinical research on aids
|
Carlyn, Marcia
|
|
1992
|
13 |
5 |
p. 408-409
2 p.
|
artikel
|
| 104 |
Parametric approaches to quality adjusted survival analysis
|
Cole, Bernard
|
|
1992
|
13 |
5 |
p. 383-384
2 p.
|
artikel
|
| 105 |
Parent: A strategy for automation of data management tasks in clinical trials and registries
|
Martin, Jeffrey P.
|
|
1992
|
13 |
5 |
p. 416-
1 p.
|
artikel
|
| 106 |
Patient charges/costs in the home intravenous antibiotic trial
|
Mather, Frances J.
|
|
1992
|
13 |
5 |
p. 396-
1 p.
|
artikel
|
| 107 |
Patient compliance as an explanatory variable in the aspirin myocardial infarction study
|
Zurakowski, David
|
|
1992
|
13 |
5 |
p. 382-
1 p.
|
artikel
|
| 108 |
Performance evaluation in multicenter clinical trials: Development of a model by the aids clinical trials group (ACTG)
|
Rosendorf, Linda L.
|
|
1992
|
13 |
5 |
p. 404-
1 p.
|
artikel
|
| 109 |
Performance evaluation of centers participating in a multicenter clinical trial group: A model developed for the community programs for clinical research on aids (CPCRA)
|
Hedderman, Michael
|
|
1992
|
13 |
5 |
p. 403-
1 p.
|
artikel
|
| 110 |
Planning for computer migration during the course of a clinical trial
|
LoPresti, Frances
|
|
1992
|
13 |
5 |
p. 400-
1 p.
|
artikel
|
| 111 |
Population screening for randomization into large scale cholesterol reduction clinical trials
|
Norrie, John
|
|
1992
|
13 |
5 |
p. 426-427
2 p.
|
artikel
|
| 112 |
Predicting noncompliance among HIV positive asymptomatic individuals in a randomized controlled clinical trial
|
Berzon, Richard
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1992
|
13 |
5 |
p. 426-
1 p.
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artikel
|
| 113 |
Predictive value of repeated measurements of CD4 lymphocyte counts on progression to aids
|
Boutitie, Florent
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1992
|
13 |
5 |
p. 378-
1 p.
|
artikel
|
| 114 |
Preliminary safety and activity evaluation of new agents for the treatment of HIV-1 infection: Recommended guidelines for trial design
|
Stein, Daniel
|
|
1992
|
13 |
5 |
p. 388-
1 p.
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artikel
|
| 115 |
Problems in assessing left ventricular function in clinical trials
|
Ahn, Sylvie
|
|
1992
|
13 |
5 |
p. 424-425
2 p.
|
artikel
|
| 116 |
Problems in drawing conclusions in barrier contraceptive clinical trials with compliance problems
|
Sharma, Inder J.
|
|
1992
|
13 |
5 |
p. 441-
1 p.
|
artikel
|
| 117 |
Prognostic indices: Who needs them?
|
Dunn, Janet A.
|
|
1992
|
13 |
5 |
p. 381-382
2 p.
|
artikel
|
| 118 |
Publication of randomized clinical trials in vision research submitted as abstracts to national ophthalmology meetings
|
Scherer, Roberta W.
|
|
1992
|
13 |
5 |
p. 421-
1 p.
|
artikel
|
| 119 |
Pursuing high quality data through structured form design
|
Remaley, Nancy
|
|
1992
|
13 |
5 |
p. 438-439
2 p.
|
artikel
|
| 120 |
Quality assurance and multicenter clinical trials
|
Koski, Beverly
|
|
1992
|
13 |
5 |
p. 430-
1 p.
|
artikel
|
| 121 |
Quality of life before and after knowledge of a trial's results
|
Fitch, Laurie L.
|
|
1992
|
13 |
5 |
p. 396-397
2 p.
|
artikel
|
| 122 |
Randomized clinical trials on medical treatment of glaucoma: Are they appropriate to guide clinical practice?
|
Rossetti, Luca
|
|
1992
|
13 |
5 |
p. 421-
1 p.
|
artikel
|
| 123 |
Randomized, three-step trial design for phase 1 study of chemopreventive agents
|
Carbone, Paul
|
|
1992
|
13 |
5 |
p. 388-
1 p.
|
artikel
|
| 124 |
Random time versus fixed time sampling in clinical trials among drug addicts
|
Jain, Ram B.
|
|
1992
|
13 |
5 |
p. 398-
1 p.
|
artikel
|
| 125 |
Rank statistics for analysis of a clinical trial with multiple events per patient: The multicenter study of hydroxyurea in sickle cell anemia (MSH)
|
McMahon, Robert P.
|
|
1992
|
13 |
5 |
p. 441-
1 p.
|
artikel
|
| 126 |
React—A hand-held computer system to facilitate clinical trials
|
Schneider, Martin J.
|
|
1992
|
13 |
5 |
p. 401-
1 p.
|
artikel
|
| 127 |
Recruitment experience in the home intravenous antibiotic trial
|
Mather, Frances J.
|
|
1992
|
13 |
5 |
p. 429-
1 p.
|
artikel
|
| 128 |
Recruitment of clinicaal centers in an investigator-initiated multicenter clinical trial
|
Howard, Virginia J.
|
|
1992
|
13 |
5 |
p. 394-
1 p.
|
artikel
|
| 129 |
Recruitment strategies in the studies of left ventricular dysfunction (SOLVD): Strategies for screening and enrollment in two concurrent but separate trials
|
Carew, Beryl D.
|
|
1992
|
13 |
5 |
p. 325-338
14 p.
|
artikel
|
| 130 |
Registry of resource centers for multicenter clinical studies
|
Fink, Nancy
|
|
1992
|
13 |
5 |
p. 433-434
2 p.
|
artikel
|
| 131 |
Regression to the mean in clinical trials with entry based on counting events
|
McMahon, Robert P.
|
|
1992
|
13 |
5 |
p. 427-
1 p.
|
artikel
|
| 132 |
Remote entry to integrated clinical project database: On-line reporting of clinical trial site visit information by clinical research associates
|
Nagle, Barbara
|
|
1992
|
13 |
5 |
p. 396-
1 p.
|
artikel
|
| 133 |
Retrospective psychometric reports are poor estimates of treatment success
|
Feine, Jocelyne S.
|
|
1992
|
13 |
5 |
p. 433-
1 p.
|
artikel
|
| 134 |
Sample size determination using an interim analysis
|
Bristol, David R.
|
|
1992
|
13 |
5 |
p. 414-
1 p.
|
artikel
|
| 135 |
Screening rules for determining blood pressure status in clinical trials: Application to the trials of hypertension prevention
|
Cook, Nancy R.
|
|
1992
|
13 |
5 |
p. 393-
1 p.
|
artikel
|
| 136 |
Selecting a RDBMS for a multi-disciplinary clinical research database
|
Wu, D.
|
|
1992
|
13 |
5 |
p. 418-419
2 p.
|
artikel
|
| 137 |
Selection of covariates in the cox model: Simulations
|
Barton, Franca
|
|
1992
|
13 |
5 |
p. 420-
1 p.
|
artikel
|
| 138 |
Simplified assessment of lab parameters in clinical trials—Basic considerations
|
Pochibradsky, Maria Grazia
|
|
1992
|
13 |
5 |
p. 413-
1 p.
|
artikel
|
| 139 |
Simpliying large trials: An example from the community programs for clinical research on aids
|
Matts, John P.
|
|
1992
|
13 |
5 |
p. 408-
1 p.
|
artikel
|
| 140 |
Simulation study comparing cumulative mean change with slope estimate summaries: Application to a comparative trial of venlafaxine, imipramine, and placebo
|
Entsuah, A.Richard
|
|
1992
|
13 |
5 |
p. 439-
1 p.
|
artikel
|
| 141 |
Social security number—An appropriate algorithm for randomization in a community hospital setting?
|
Blackhurst, Dawn W.
|
|
1992
|
13 |
5 |
p. 412-
1 p.
|
artikel
|
| 142 |
Society for clinical trials student scholarship program
|
|
|
1992
|
13 |
5 |
p. 443-
1 p.
|
artikel
|
| 143 |
Standardization description of dose-ranging trial protocol
|
Boissel, Jean-Pierre
|
|
1992
|
13 |
5 |
p. 430-431
2 p.
|
artikel
|
| 144 |
Standing committees
|
|
|
1992
|
13 |
5 |
p. 355-
1 p.
|
artikel
|
| 145 |
Statistical considerations in monitoring the systolic hypertension in the elderly program
|
Davis, Barry R.
|
|
1992
|
13 |
5 |
p. 414-
1 p.
|
artikel
|
| 146 |
Strategies for educating and training clinicians to conduct community-based research: A report from the community programs for clinical research on aids
|
Maiatico, Geraldine
|
|
1992
|
13 |
5 |
p. 402-
1 p.
|
artikel
|
| 147 |
Subject file checklists to facilitate clinical trial close-out activities
|
Pelusio, Rita M.
|
|
1992
|
13 |
5 |
p. 438-
1 p.
|
artikel
|
| 148 |
Subjective quality of life assessment: A new instrument, the “SQLP”
|
Gerin, Paul
|
|
1992
|
13 |
5 |
p. 397-
1 p.
|
artikel
|
| 149 |
Techniques for editing longitudinal growth data
|
Barton, Bruce
|
|
1992
|
13 |
5 |
p. 438-
1 p.
|
artikel
|
| 150 |
Termination issues in long-term clinical trial research
|
Jensen, Judith
|
|
1992
|
13 |
5 |
p. 425-
1 p.
|
artikel
|
| 151 |
The analysis of a single-patient efficacy trial of an investigational antiepileptic drug
|
Sahlroot, J.Todd
|
|
1992
|
13 |
5 |
p. 410-
1 p.
|
artikel
|
| 152 |
The analysis of incomplete data in the three-period two-treatment crossover design for clinical trials
|
Richardson, Barbra
|
|
1992
|
13 |
5 |
p. 381-
1 p.
|
artikel
|
| 153 |
The development of a national perinatal clinical trials network in Canada: The first step
|
Hannah, Mary
|
|
1992
|
13 |
5 |
p. 407-
1 p.
|
artikel
|
| 154 |
The development of data collection tools to assist in protocol management
|
Houston, C.
|
|
1992
|
13 |
5 |
p. 415-416
2 p.
|
artikel
|
| 155 |
The difficulties in the data management of recurrent and transient events in prospective randomized clinical trials: Example from a randomized trial comparing two different brachytherapy dose rates in gynaecological cancer
|
Bouzy, Jeannine
|
|
1992
|
13 |
5 |
p. 434-
1 p.
|
artikel
|
| 156 |
The importance of quality and accuracy in the conduct of clinical trials: EORTC quality assurance measures
|
Vantongelen, K.
|
|
1992
|
13 |
5 |
p. 400-401
2 p.
|
artikel
|
| 157 |
The measurement of visual analogue scale data is not a burden
|
Palmer, Michael J.
|
|
1992
|
13 |
5 |
p. 435-
1 p.
|
artikel
|
| 158 |
The paradox of rapid accrual
|
Palmer, Michael J.
|
|
1992
|
13 |
5 |
p. 428-
1 p.
|
artikel
|
| 159 |
The use of computer-assisted instruction (CAI) for protocol training
|
Rolnick, Sharon
|
|
1992
|
13 |
5 |
p. 402-
1 p.
|
artikel
|
| 160 |
The use of focus groups in the design of cholesterol education intervention programs
|
Masters, Rebecca B.
|
|
1992
|
13 |
5 |
p. 424-
1 p.
|
artikel
|
| 161 |
Thirteenth annual meeting of the society for clinical trials
|
|
|
1992
|
13 |
5 |
p. 356-376
21 p.
|
artikel
|
| 162 |
Toxicity grading systems
|
Franklin, Hilary
|
|
1992
|
13 |
5 |
p. 385-
1 p.
|
artikel
|
| 163 |
Understanding physician accrual of eligible patients to North American symptomatic carotid endarterectomy trial (NASCET)
|
Taylor, Kathryn M.
|
|
1992
|
13 |
5 |
p. 392-
1 p.
|
artikel
|
| 164 |
Use of a relational database to track correspondence regarding requested corrections to case data records
|
McGrath, P.D.
|
|
1992
|
13 |
5 |
p. 418-
1 p.
|
artikel
|
| 165 |
Using SAS to monitor trial supplies: Experience gained in a multicentre trial
|
Gould, Caroline A.L.
|
|
1992
|
13 |
5 |
p. 439-
1 p.
|
artikel
|
| 166 |
Variation in resource center workload and productivity over a 13-year period
|
Hawkins, Barbara S.
|
|
1992
|
13 |
5 |
p. 433-
1 p.
|
artikel
|
| 167 |
When should randomization to untreated control groups stop?
|
Chalmers, Thomas
|
|
1992
|
13 |
5 |
p. 380-
1 p.
|
artikel
|
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