| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A comparative analysis of treatment balance utilizing sequential assignment and other randomization schemes
|
Gross Fisher, Susan
|
|
1986
|
7 |
3 |
p. 236-
1 p.
|
artikel
|
| 2 |
A comparison of form design elements affecting data entry quality: Results of two large multicenter trials
|
Pollizzi, Sue
|
|
1986
|
7 |
3 |
p. 257-
1 p.
|
artikel
|
| 3 |
A comparison of functional status measures in chronic lung disease: Data from a randomized control trial
|
Keller, J.L.
|
|
1986
|
7 |
3 |
p. 233-
1 p.
|
artikel
|
| 4 |
Adherence to protocol over the course of a clinical trial
|
Michelson, Seth
|
|
1986
|
7 |
3 |
p. 243-
1 p.
|
artikel
|
| 5 |
A human volunteer rhinovirus (RV) transmission model—a new clinical trial design for evaluation of antiviral prophylaxis
|
Meschievitz, C.
|
|
1986
|
7 |
3 |
p. 249-
1 p.
|
artikel
|
| 6 |
A “life table” that handles recovery and arbitrarily many states of being
|
Hillis, Argye
|
|
1986
|
7 |
3 |
p. 246-
1 p.
|
artikel
|
| 7 |
A method for the evaluation of compliance in clinical trials
|
Villa, Erica
|
|
1986
|
7 |
3 |
p. 251-
1 p.
|
artikel
|
| 8 |
“A mixed blessing”: Informed consent for randomized clinical trials
|
Taylor, Kathryn M.
|
|
1986
|
7 |
3 |
p. 240-
1 p.
|
artikel
|
| 9 |
An AIDS registry for epidemiology and clinical trials management
|
Vranizan, K.
|
|
1986
|
7 |
3 |
p. 255-
1 p.
|
artikel
|
| 10 |
Analysis of crossover studies with multiple baseline measurements
|
Moreadith, Connie W.
|
|
1986
|
7 |
3 |
p. 253-
1 p.
|
artikel
|
| 11 |
Analysis of recurrent events based on random interval count data
|
Thall, Peter F.
|
|
1986
|
7 |
3 |
p. 237-
1 p.
|
artikel
|
| 12 |
Analysis of repeated measures when the assessment procedure is also therapeutic
|
Gelber, Richard D.
|
|
1986
|
7 |
3 |
p. 237-
1 p.
|
artikel
|
| 13 |
An overview of trials of pharmacologic therapy of mild hypertension
|
Hebert, Pat
|
|
1986
|
7 |
3 |
p. 239-
1 p.
|
artikel
|
| 14 |
Archives for data and documents from completed clinical trials: How are they maintained and how they been used?
|
Hawkins, Barbara S.
|
|
1986
|
7 |
3 |
p. 244-
1 p.
|
artikel
|
| 15 |
A review of statistical procedures when establishing equivalence between treatments
|
Com-Nougué, Catherine
|
|
1986
|
7 |
3 |
p. 245-
1 p.
|
artikel
|
| 16 |
Assessment of potential bias of an operational team in a large-scale long-term multicenter trial
|
de Sola Pinto, Martine
|
|
1986
|
7 |
3 |
p. 232-
1 p.
|
artikel
|
| 17 |
A standardized approach to the tabulation and statistical evaluation of laboratory data
|
Quinn, Joseph B.
|
|
1986
|
7 |
3 |
p. 258-
1 p.
|
artikel
|
| 18 |
A technique for evaluating clinical equivalence
|
Summerfelt, Ann
|
|
1986
|
7 |
3 |
p. 250-
1 p.
|
artikel
|
| 19 |
A “turnkey” system for clinical trial data quality control
|
Major, Robert
|
|
1986
|
7 |
3 |
p. 228-
1 p.
|
artikel
|
| 20 |
Automatic stratification procedure for assessment of interaction and confounding effects
|
Siu, Cynthia
|
|
1986
|
7 |
3 |
p. 253-
1 p.
|
artikel
|
| 21 |
Biostatistical microcomputing in pascal
|
Sylvester, Richard
|
|
1986
|
7 |
3 |
p. 261-263
3 p.
|
artikel
|
| 22 |
Centralization versus decentralization management specific to clinical research associates in the pharmaceutical industry
|
Jane Baine, Mary
|
|
1986
|
7 |
3 |
p. 256-
1 p.
|
artikel
|
| 23 |
Centralized 10–15 year follow-up by the coordinating center in the VA Coronary bypass surgery study—design and results
|
Peduzzi, Peter
|
|
1986
|
7 |
3 |
p. 244-
1 p.
|
artikel
|
| 24 |
Clinical trial program management using a microcomputer
|
Hurden, Eric L.
|
|
1986
|
7 |
3 |
p. 256-
1 p.
|
artikel
|
| 25 |
Clinical trial program management using a microcomputer
|
Hurden, Eric L.
|
|
1986
|
7 |
3 |
p. 234-
1 p.
|
artikel
|
| 26 |
Cluster analysis: Classification of color vision test results from the ETDRS and other possible applications
|
Barton, Franca
|
|
1986
|
7 |
3 |
p. 230-
1 p.
|
artikel
|
| 27 |
Communication network in a multicenter trial
|
Seif, Diane
|
|
1986
|
7 |
3 |
p. 254-
1 p.
|
artikel
|
| 28 |
Comparison of two urine tests (drug marker vs. metabolite) to measure compliance with disulfiram
|
Lee, Kelvin K.
|
|
1986
|
7 |
3 |
p. 252-
1 p.
|
artikel
|
| 29 |
Compound endpoints in clinical trials
|
Terrin, Michael
|
|
1986
|
7 |
3 |
p. 250-
1 p.
|
artikel
|
| 30 |
Confoundedness of the odds ratio in randomized clinical trials
|
Tijssen, Jan G.P.
|
|
1986
|
7 |
3 |
p. 238-
1 p.
|
artikel
|
| 31 |
Considerations of nominal significance subsequent to various treatment allocation procedures in clinical trials
|
Kalish, Leslie A.
|
|
1986
|
7 |
3 |
p. 259-
1 p.
|
artikel
|
| 32 |
Converting relative risks to absolute risks: A graphical approach for breast cancer and heart disease
|
Dupont, William D.
|
|
1986
|
7 |
3 |
p. 238-
1 p.
|
artikel
|
| 33 |
Cost-effectiveness analysis in clinical trials
|
Chan, Yick-Kwong
|
|
1986
|
7 |
3 |
p. 231-
1 p.
|
artikel
|
| 34 |
Data management and quality control in the veterans administration cooperative study 213: Treatment of mild hypertension in the aged
|
Reda, Dominic J.
|
|
1986
|
7 |
3 |
p. 256-
1 p.
|
artikel
|
| 35 |
Data management: Quantification, evaluation, and control
|
Barker, Christopher M.
|
|
1986
|
7 |
3 |
p. 259-
1 p.
|
artikel
|
| 36 |
Design, development, and implementation of a data processing system for multiple controlled trials and epidemiologic studies
|
|
|
1986
|
7 |
3 |
p. 266-
1 p.
|
artikel
|
| 37 |
Designing computerized edit systems for trials involving medical management protocols
|
Canner, Joseph
|
|
1986
|
7 |
3 |
p. 227-
1 p.
|
artikel
|
| 38 |
Diabetes control and complications trial (DCCT): Results of the feasibility study and design of the full-scale clinical trial
|
Siebert, Carolyn
|
|
1986
|
7 |
3 |
p. 235-
1 p.
|
artikel
|
| 39 |
Early patent ductus arteriosis ligation, a prospective randomized controlled trial
|
Crouse, Dennis
|
|
1986
|
7 |
3 |
p. 249-
1 p.
|
artikel
|
| 40 |
Efficient designs for randomized trials with response as an endpoint
|
Wieand, Sam
|
|
1986
|
7 |
3 |
p. 236-
1 p.
|
artikel
|
| 41 |
Estimation of treatment effect in the presence of chance incomparability at baseline: A detailed example
|
Tijssen, Jan G.P.
|
|
1986
|
7 |
3 |
p. 236-
1 p.
|
artikel
|
| 42 |
Facilitating review and correction of complex clinical data in cardiovascular clinical trials
|
Gilkerson, Ellen
|
|
1986
|
7 |
3 |
p. 227-
1 p.
|
artikel
|
| 43 |
Factors influencing patient evaluability in anti-infective clinical trials
|
Hosutt, Jean A.
|
|
1986
|
7 |
3 |
p. 251-
1 p.
|
artikel
|
| 44 |
How to disseminate clinical trial results: Physician views
|
Schucker, Beth
|
|
1986
|
7 |
3 |
p. 255-
1 p.
|
artikel
|
| 45 |
How to establish equivalence between treatments: A trial of the international society of pediatric oncology (S.I.O.P.) on nephroblastoma
|
Rodary, Chantal
|
|
1986
|
7 |
3 |
p. 246-
1 p.
|
artikel
|
| 46 |
Human experimentation: A guided step into the unknown
|
Hawkins, Barbara S.
|
|
1986
|
7 |
3 |
p. 260-261
2 p.
|
artikel
|
| 47 |
Imputation when nearly half the data are missing
|
Van Natta, Pearl
|
|
1986
|
7 |
3 |
p. 229-
1 p.
|
artikel
|
| 48 |
Influence of diagnostic certainty upon the results of a field trial
|
Meister, W.
|
|
1986
|
7 |
3 |
p. 240-
1 p.
|
artikel
|
| 49 |
Influence of impending “overview analysis” and “consensus conference” results on clinical research: The Nutrition Adjuvant Study (NAS) experience
|
Chlebowski, Rowan T.
|
|
1986
|
7 |
3 |
p. 241-
1 p.
|
artikel
|
| 50 |
Interrater reliability of SAFTEE in psychopharmacologic clinical trials
|
Jacobson, Alan Frank
|
|
1986
|
7 |
3 |
p. 230-
1 p.
|
artikel
|
| 51 |
Issues in the organization of reading centers in multicentered clinical trials
|
Sternberg, Alice L.
|
|
1986
|
7 |
3 |
p. 244-
1 p.
|
artikel
|
| 52 |
Logistical issues in conducting multicontinent clinical trials
|
Price, Karen
|
|
1986
|
7 |
3 |
p. 254-
1 p.
|
artikel
|
| 53 |
Measuring electrolyte excretion from random overnight urine collections
|
Hiller, Janet
|
|
1986
|
7 |
3 |
p. 230-
1 p.
|
artikel
|
| 54 |
Mechanism for double-blinding a randomized trial of short- vs. long-course intravenous heparin therapy for venous thrombosis
|
Raskob, G.
|
|
1986
|
7 |
3 |
p. 248-
1 p.
|
artikel
|
| 55 |
Meta-analysis in clinical trials
|
DerSimonian, Rebecca
|
|
1986
|
7 |
3 |
p. 177-188
12 p.
|
artikel
|
| 56 |
Meta analysis of unpublished subgroups data, logistical and statistical problems: The experience of the beta-blocker pooling project (BBPP)
|
Leizorovicz, A.
|
|
1986
|
7 |
3 |
p. 239-
1 p.
|
artikel
|
| 57 |
Microcomputers in clinical trials for dietary management
|
Powers, Sandra N.
|
|
1986
|
7 |
3 |
p. 234-
1 p.
|
artikel
|
| 58 |
Misinterpretation of graphical goodness of fit tests used in medical trials
|
Elandt-Johnson, Regina C.
|
|
1986
|
7 |
3 |
p. 247-
1 p.
|
artikel
|
| 59 |
Missing data—A patient or clinical center problem?
|
Tierney, Camlin
|
|
1986
|
7 |
3 |
p. 228-
1 p.
|
artikel
|
| 60 |
Modeling accrual, cost, and paper flow in randomized clinical trials
|
Piantadosi, Steven
|
|
1986
|
7 |
3 |
p. 243-
1 p.
|
artikel
|
| 61 |
New measures of drug efficacy: Significant other reports
|
Schwartz, Gerri E.
|
|
1986
|
7 |
3 |
p. 247-
1 p.
|
artikel
|
| 62 |
Omitted covariates in proportional hazards regression
|
Banks, Steven M.
|
|
1986
|
7 |
3 |
p. 247-
1 p.
|
artikel
|
| 63 |
On the power of two tests for qualitative interaction
|
Piantadosi, Steven
|
|
1986
|
7 |
3 |
p. 230-
1 p.
|
artikel
|
| 64 |
Organization and management of two randomized clinical trials in the people's Republic of China
|
Tangrea, Joseph A.
|
|
1986
|
7 |
3 |
p. 254-
1 p.
|
artikel
|
| 65 |
Overcoming bias in a clinical trial
|
Ziliotto, Cecily
|
|
1986
|
7 |
3 |
p. 232-
1 p.
|
artikel
|
| 66 |
Patient entry into clinical trials
|
van der Linden, Els
|
|
1986
|
7 |
3 |
p. 240-
1 p.
|
artikel
|
| 67 |
Patient management and stopping rule in a chronic lymphocytic leukemia randomized clinical trial
|
Chastang, Claude
|
|
1986
|
7 |
3 |
p. 240-
1 p.
|
artikel
|
| 68 |
Perusing the literature
|
Hawkins, Barbara S.
|
|
1986
|
7 |
3 |
p. 200-213
14 p.
|
artikel
|
| 69 |
Prerandomization adherence aids for clinical trials
|
Probstfield, J.
|
|
1986
|
7 |
3 |
p. 242-
1 p.
|
artikel
|
| 70 |
Problems in screening for obese mild hypertension, part i: Design issues
|
Haggerty, Patricia
|
|
1986
|
7 |
3 |
p. 232-
1 p.
|
artikel
|
| 71 |
Properties of three sequential methods in randomized clinical trials with a censored response criterion
|
Benichou, Jacques
|
|
1986
|
7 |
3 |
p. 237-
1 p.
|
artikel
|
| 72 |
Protocol deviations due to side effects in the SHEP pilot study
|
Feigal, David
|
|
1986
|
7 |
3 |
p. 252-
1 p.
|
artikel
|
| 73 |
Psychosocial factors influencing patient entry and refusal in clinical cancer trials
|
van der Velden, J.W.
|
|
1986
|
7 |
3 |
p. 251-
1 p.
|
artikel
|
| 74 |
Quality analysis of randomized control trials (RCT) of the treatment of advanced ovarian cancer (AOC)
|
Marsoni, S.
|
|
1986
|
7 |
3 |
p. 239-
1 p.
|
artikel
|
| 75 |
Quality of life as an outcome in long-term clinical trials
|
van Es, Gerrit-Anne
|
|
1986
|
7 |
3 |
p. 253-
1 p.
|
artikel
|
| 76 |
Randomized design and analysis of randomized clinical trials
|
Blumenstein, Brent A.
|
|
1986
|
7 |
3 |
p. 235-
1 p.
|
artikel
|
| 77 |
Reliability and validity of a quality of life measure for lung and colon cancer patients
|
Ryan, Lucille S.
|
|
1986
|
7 |
3 |
p. 258-
1 p.
|
artikel
|
| 78 |
Restricted mean life with adjustment for covariates
|
Karrison, Theodore
|
|
1986
|
7 |
3 |
p. 247-
1 p.
|
artikel
|
| 79 |
Robert S. Gordon, Jr., M.D., M.H.S. 1926–1985
|
|
|
1986
|
7 |
3 |
p. 265-
1 p.
|
artikel
|
| 80 |
Sample size considerations in vaccine trials
|
Blackwelder, William C.
|
|
1986
|
7 |
3 |
p. 253-
1 p.
|
artikel
|
| 81 |
Sample size determination in clinical trials with time-dependent rates of losses and noncompliance
|
Lakatos, Edward
|
|
1986
|
7 |
3 |
p. 189-199
11 p.
|
artikel
|
| 82 |
Sample size in survival studies
|
Elashoff, Robert
|
|
1986
|
7 |
3 |
p. 245-
1 p.
|
artikel
|
| 83 |
Sealed mailer security
|
Hobbins, Thomas E.
|
|
1986
|
7 |
3 |
p. 254-
1 p.
|
artikel
|
| 84 |
Seventh Annual Meeting Society for Clinical Trials
|
|
|
1986
|
7 |
3 |
p. 214-226
13 p.
|
artikel
|
| 85 |
Simulation methods for sample size in trials with arbitrary hazards
|
Piantadosi, Steven
|
|
1986
|
7 |
3 |
p. 246-
1 p.
|
artikel
|
| 86 |
Some issues in the analysis of changes in lipid variables during chronic drug therapy
|
Horton, J.
|
|
1986
|
7 |
3 |
p. 258-
1 p.
|
artikel
|
| 87 |
Stopping medications in a placebo-controlled trial in the elderly: The SHEP pilot study
|
Black, Dennis
|
|
1986
|
7 |
3 |
p. 252-
1 p.
|
artikel
|
| 88 |
Surrogate endpoint use in cardiovascular clinical trials
|
Probstfield, J.L.
|
|
1986
|
7 |
3 |
p. 241-
1 p.
|
artikel
|
| 89 |
Systolic hypertension in the elderly program (SHEP) pilot study: Predictors of cardiovascular (CV) events
|
Siegel, David
|
|
1986
|
7 |
3 |
p. 250-
1 p.
|
artikel
|
| 90 |
The beta error in clinical trials in emergency medicine
|
Brown, Charles G.
|
|
1986
|
7 |
3 |
p. 238-
1 p.
|
artikel
|
| 91 |
The design of V-HEFT II: Rerandomization of V-HEFT I survivors
|
Archibald, Donald G.
|
|
1986
|
7 |
3 |
p. 248-
1 p.
|
artikel
|
| 92 |
The effective use of a local area network for the data management of clinical and nutritional data from a multicenter clinical trial
|
Sayre, James
|
|
1986
|
7 |
3 |
p. 234-
1 p.
|
artikel
|
| 93 |
The effect of method of ascertainment on frequency of reported side effects in clinical trials
|
Levine, Jerome
|
|
1986
|
7 |
3 |
p. 231-
1 p.
|
artikel
|
| 94 |
The impact of national treatment guidelines for the treatment of breast cancer in Italy
|
Liberati, A.
|
|
1986
|
7 |
3 |
p. 243-
1 p.
|
artikel
|
| 95 |
The impact of the German ALL/AUL-study on the treatment of acute leukemia
|
Hasford, Joerg
|
|
1986
|
7 |
3 |
p. 257-
1 p.
|
artikel
|
| 96 |
The multicenter trial of cryotherapy for retinopathy of prematurity: Design features
|
Hardy, Robert J.
|
|
1986
|
7 |
3 |
p. 235-
1 p.
|
artikel
|
| 97 |
The pitfalls of incomplete data set analysis
|
|
|
1986
|
7 |
3 |
p. 229-
1 p.
|
artikel
|
| 98 |
The routine use of winsorization in data monitoring reports to reduce the effects of influential observations
|
Tonascia, James
|
|
1986
|
7 |
3 |
p. 229-
1 p.
|
artikel
|
| 99 |
The trial coordinator's role in the diabetes control and complications trial (DCCT)
|
Kruger, Davida
|
|
1986
|
7 |
3 |
p. 257-
1 p.
|
artikel
|
| 100 |
The University coordinated drug trial: An organizational schematic
|
Annechiarico, Robert
|
|
1986
|
7 |
3 |
p. 255-
1 p.
|
artikel
|
| 101 |
The use of a run-in before randomization
|
Lang, Janet M.
|
|
1986
|
7 |
3 |
p. 242-
1 p.
|
artikel
|
| 102 |
Translation of photographic documentation into numeric data
|
Chamberlin, Judith A.
|
|
1986
|
7 |
3 |
p. 249-
1 p.
|
artikel
|
| 103 |
Turnover among clinical coordinators in two multicenter clinical trials
|
Optican, Donna C.
|
|
1986
|
7 |
3 |
p. 257-
1 p.
|
artikel
|
| 104 |
Use of a relational data base management system
|
Reis, Janet
|
|
1986
|
7 |
3 |
p. 233-
1 p.
|
artikel
|
| 105 |
Use of cox time-dependent regression to adjust for factors confounded with treatment effect in a randomized clinical trial
|
Gillespie, B.W.
|
|
1986
|
7 |
3 |
p. 259-
1 p.
|
artikel
|
| 106 |
Use of mortality of all screened patients to check the relevance of study population as regards to the target population in intervention studies
|
Boissel, J.P.
|
|
1986
|
7 |
3 |
p. 242-
1 p.
|
artikel
|
| 107 |
Use of the national death index in cancer studies
|
Patterson, Blossom H.
|
|
1986
|
7 |
3 |
p. 249-
1 p.
|
artikel
|
| 108 |
Using an expert system to automate the element of clinical judgment in data analyses
|
Long, J.M.
|
|
1986
|
7 |
3 |
p. 233-
1 p.
|
artikel
|
| 109 |
Women as participants in cardiovascular trials
|
MacMahon, S.
|
|
1986
|
7 |
3 |
p. 242-
1 p.
|
artikel
|
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