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                             128 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A cohort study of controlled trials initially reported as abstracts 1989
10 3 p. 319-
1 p.
artikel
2 A coordinated system for randomizing patients to treatments and producing labels for clinical trials Main, David
1989
10 3 p. 335-336
2 p.
artikel
3 A coordinating center's role in blinding of medication Randall, A.M.Y.
1989
10 3 p. 338-
1 p.
artikel
4 A critique of recent research on the two-treatment crossover design Fleiss, Joseph L.
1989
10 3 p. 237-243
7 p.
artikel
5 Adherence to Medication dosage schedules 1989
10 3 p. 333-334
2 p.
artikel
6 A distributed data entry system Paul Beattie, W.
1989
10 3 p. 343-
1 p.
artikel
7 Advanced multicenter research (A.M.R.) Rago, Salvatore
1989
10 3 p. 339-340
2 p.
artikel
8 Adverse drug reactions in clinical trials Day, Philip
1989
10 3 p. 336-
1 p.
artikel
9 Adverse effects as primary endpoint: The hypren-trial experience 1989
10 3 p. 329-
1 p.
artikel
10 A focus-based database system for clinical trials Glenn, Bruce
1989
10 3 p. 341-
1 p.
artikel
11 A local area network (LAN) based protocol tracking and information systems (PTIS) for cancer clinical trials Multhauf, Phyllis M.
1989
10 3 p. 341-
1 p.
artikel
12 A multi-center phase I trial of chemotherapy in operable breast cancer 1989
10 3 p. 323-
1 p.
artikel
13 An approach to summarizing lab data from multicenter trials 1989
10 3 p. 317-
1 p.
artikel
14 An expert system for documenting DSM-III_R schizophrenia related diagnoses Levine, Jerome
1989
10 3 p. 344-345
2 p.
artikel
15 An N of 1 service: How well does it work? 1989
10 3 p. 333-
1 p.
artikel
16 Announcement 1989
10 3 p. 356-
1 p.
artikel
17 A randomized, double-blind study of cemented (C) versus non-cemented (NC) hip prostheses (HP) 1989
10 3 p. 329-
1 p.
artikel
18 Are coding systems to handle text-data in clinical trials still necessary? 1989
10 3 p. 326-
1 p.
artikel
19 Are (placebo) run-in periods necessary in a drug trial in a chronic disorder? Tijssen, J.G.P.
1989
10 3 p. 334-
1 p.
artikel
20 A sequential test for a phase II efficacy study 1989
10 3 p. 319-320
2 p.
artikel
21 A simple predictive model of leucopenia induced by cytotoxic anticancer drugs: The example of 4′-O-tetrahydropyranyl-doxorubicin (THP-ADM). Overview of 8 phase II studies conducted by the EORTC Clinical Screening Group (CSG) 1989
10 3 p. 317-318
2 p.
artikel
22 Assessing antiarrhythmic drug efficacy in considering all forms of arrhythmias simultaneously Ulm, K.
1989
10 3 p. 347-
1 p.
artikel
23 Assessing the effect of stopping therapy Anderson, Sharon
1989
10 3 p. 348-
1 p.
artikel
24 A standard phase IV protocol Norton, John W.
1989
10 3 p. 351-
1 p.
artikel
25 A “weighted” rank sum test Hallstrom, Alfred P.
1989
10 3 p. 345-
1 p.
artikel
26 Bayesian methods for analying treatment-by-subset interaction in clinical trials 1989
10 3 p. 331-
1 p.
artikel
27 Caffeine effects on calcium physiology in a crossover study: Issues in methods and analysis Stegman, Mary Ruth
1989
10 3 p. 350-
1 p.
artikel
28 Choosing covariates in the analysis of clinical trials 1989
10 3 p. 320-
1 p.
artikel
29 Clinical judgement and centralized data management Boone, Donna
1989
10 3 p. 339-
1 p.
artikel
30 Clinical trials can improve patient care and, at the same time contain costs 1989
10 3 p. 332-
1 p.
artikel
31 Communication strategies for multi-center clinical trials: The BARI hotline Sutton-Tyrrell, Kim
1989
10 3 p. 343-
1 p.
artikel
32 Comparison of errors in body surface area and initial chemotherapy doses in five clinical trials J. Palmer, Michael
1989
10 3 p. 351-
1 p.
artikel
33 Computerized follow-up program for large clinical trials Ahn, Sylvie
1989
10 3 p. 336-
1 p.
artikel
34 Conducting a randomized cancer control trial in cooperative cancer treatment networks 1989
10 3 p. 325-
1 p.
artikel
35 Considerations for the meta-analysis of randomized clinical trials Boissel, Jean-Pierre
1989
10 3 p. 254-281
28 p.
artikel
36 Criteria for bleeding events in a heart valve replacement trial Giroux Klimek, M.
1989
10 3 p. 338-
1 p.
artikel
37 CTS: A clinical trials simulator Wayne Taylor, D.
1989
10 3 p. 343-344
2 p.
artikel
38 Data editing and updating under centralized and distributed systems Owen, Walter W.
1989
10 3 p. 342-
1 p.
artikel
39 Defining the universe of patients 1989
10 3 p. 324-
1 p.
artikel
40 Design and implementation of the optic neuritis treatment trial Cleary, Patricia A.
1989
10 3 p. 350-
1 p.
artikel
41 Designing longitudinal studies in progressive renal disease 1989
10 3 p. 316-
1 p.
artikel
42 Design issues related to longitudinal studies of progressive dichotomous outcome measures that are subject to misdiagnosis 1989
10 3 p. 317-
1 p.
artikel
43 Design of a randomized clinical trial with slope as the outcome: The modification of diet in renal disease (MDRD) study 1989
10 3 p. 316-
1 p.
artikel
44 Design of a two-tiered clinical trial: Studies of left ventricular dysfunction 1989
10 3 p. 323-
1 p.
artikel
45 Design of the POSCH kidney stone trial 1989
10 3 p. 323-
1 p.
artikel
46 Development of a composite index as a primary outcome measure in a clinical trial 1989
10 3 p. 328-329
2 p.
artikel
47 Differences in categorization of morbidity and mortality event variables between study coordinators and endpoint review subcommittees in the Multicenter Diltiazem Post-infarction Trial (MDPIT) 1989
10 3 p. 328-
1 p.
artikel
48 Direct data entry using a digitizing tablet in psychopharmacology clinical trials Levine, Jerome
1989
10 3 p. 344-
1 p.
artikel
49 Distributed data entry and electronic mail in the ONTT, a multicenter clinical trial Campbell, Steven T.
1989
10 3 p. 342-343
2 p.
artikel
50 Distributed data entry in the AIDS clinical trials group van der Horst, Charles
1989
10 3 p. 340-341
2 p.
artikel
51 Distributed randomization in multicenter clinical trials using microcomputer control Youngblood, Marston E.
1989
10 3 p. 340-
1 p.
artikel
52 Doctors as pertinent information receptors 1989
10 3 p. 333-
1 p.
artikel
53 Dosimetry review process for head and neck (H&N) cancer trials conducted by radiation therapy oncology group (RTOG) Pajak, Thomas F.
1989
10 3 p. 337-
1 p.
artikel
54 Eleventh annual meeting of the society for clinical trials 1989
10 3 p. 355-
1 p.
artikel
55 Ensuring the ethical conduct of cooperative clinical trials 1989
10 3 p. 332-
1 p.
artikel
56 Erratum 1989
10 3 p. 356-
1 p.
artikel
57 Estimating positive predictive value from a regression model: Screening with a non-invasive test 1989
10 3 p. 325-326
2 p.
artikel
58 Estimation of the coefficient of variation from laboratory analysis of split specimens Connett, John E.
1989
10 3 p. 348-
1 p.
artikel
59 Estimation of time to complete prevention trials when data are monitored 1989
10 3 p. 318-
1 p.
artikel
60 Ethical considerations in the design and conduct of randomized clinical trials in patients with HIV infection 1989
10 3 p. 332-
1 p.
artikel
61 Ethics, power and signigicance testing in randomized play-the-winner trials: A review of one study 1989
10 3 p. 319-
1 p.
artikel
62 Eventcharts: Visualizing survival and other timed event data Goldman, A.I.
1989
10 3 p. 346-
1 p.
artikel
63 Exact sample size calculations for 2 × 2 comparative trials when the outcome proportions are small Thomas, Ronald G.
1989
10 3 p. 347-
1 p.
artikel
64 Free reprints to increase the return of follow-up questionnaires Hughes, John R.
1989
10 3 p. 352-
1 p.
artikel
65 How many stratification factors can a study's randomization support? 1989
10 3 p. 331-
1 p.
artikel
66 Improving data quality on randomized clinical trials 1989
10 3 p. 327-
1 p.
artikel
67 Interim analysis through an independent data monitoring board 1989
10 3 p. 326-
1 p.
artikel
68 Iron supplementation during pregnancy—experiences of a randomized trial relying on health service personnel Hemminki, Elina
1989
10 3 p. 290-298
9 p.
artikel
69 Issues in effeciency and reliability in trials using surrogate endpoints 1989
10 3 p. 328-
1 p.
artikel
70 Issues in the design and analysis of clinical trials of non-bronchodilating anti-asthma drugs Uryniak, Thomas J.
1989
10 3 p. 335-
1 p.
artikel
71 Issues in the design and management of pre-hospital clinical trials: The MITI experience 1989
10 3 p. 333-
1 p.
artikel
72 Jackknifing the Cox regression estimator 1989
10 3 p. 330-
1 p.
artikel
73 Kendall's Tau and tests for trend in laboratory data Wong, Rodney M.
1989
10 3 p. 347-
1 p.
artikel
74 Management of data queries and responses with a query database in a multicenter clinical trial with distributed data entry 1989
10 3 p. 327-328
2 p.
artikel
75 Management of multi-center trials: A comparison of investigator initiated studies and other administrative models Dean Surbey, P.
1989
10 3 p. 337-
1 p.
artikel
76 Methodological quality of 290 randomized trials (RCTs) in the healing of duodenal ulcer 1989
10 3 p. 318-319
2 p.
artikel
77 Methods for detecting mislabeled data from multiple sites per patient Maguire, Maureen G.
1989
10 3 p. 354-
1 p.
artikel
78 Monitoring compliance and contamination in a chemoprevention trial Skingley, Peter
1989
10 3 p. 353-354
2 p.
artikel
79 Multiple corresponding analysis: An illustrative multivariate method applied to EORTC clinical trials Van Glabbeke, M.
1989
10 3 p. 345-346
2 p.
artikel
80 Neglect of aged in clinical trials Kannry, J.L.
1989
10 3 p. 348-
1 p.
artikel
81 Nonparametric analysis of covariance for comparing change in randomized studies with baseline values subject to error 1989
10 3 p. 330-331
2 p.
artikel
82 Operational aspects of the early termination of the multicenter trial of cryotherapy for retinopathy of prematurity 1989
10 3 p. 320-321
2 p.
artikel
83 Patient and Clinic factors predictive of missed visits and inactive status in a clinical trial Blackhurst, Dawn W.
1989
10 3 p. 335-
1 p.
artikel
84 Permanent discontinuation of study drugs in long-term clinical trials Sicurella, Jane
1989
10 3 p. 338-
1 p.
artikel
85 Permutation logrank test in controlled clinical trials 1989
10 3 p. 321-
1 p.
artikel
86 Philosophers assess randomized clinical trials: The need for dialogue Miké, Valerie
1989
10 3 p. 244-253
10 p.
artikel
87 Progression of carotid atherosclerotic plaque as an endpoint in a clinical trial: The multicenter isradipine diuretic atherosclerosis study (MIDAS) Byington, Robert P.
1989
10 3 p. 349-
1 p.
artikel
88 Proposed clinical trial of multivitamin use for the prevention of neural tube defects in China 1989
10 3 p. 322-
1 p.
artikel
89 Quality control of transfer of data in clinical trials 1989
10 3 p. 327-
1 p.
artikel
90 Quality of life in stage 2 breast cancer patients measured by a time trade off method Kestle, J.
1989
10 3 p. 350-
1 p.
artikel
91 Quantifying ascertainment bias in vaccine efficacy trials 1989
10 3 p. 324-
1 p.
artikel
92 Randomization with a pocket-computer: A surrogate device when central randomization is not possible 1989
10 3 p. 318-
1 p.
artikel
93 Rationale and design of a randomized clinical trial on postinfarction survival and ventricular enlargement 1989
10 3 p. 329-330
2 p.
artikel
94 Recruitment in private versus academic primary care settings Hughes, John R.
1989
10 3 p. 352-
1 p.
artikel
95 Recruitment in the lung health study (LHS) Connett, John
1989
10 3 p. 353-
1 p.
artikel
96 Recruitment techniques in an ongoing trial Hewson, Sheila A.
1989
10 3 p. 353-
1 p.
artikel
97 Sample sizes for constructing confidence intervals and testing hypotheses Bristol, David R.
1989
10 3 p. 345-
1 p.
artikel
98 Site visit methodology in a VA cooperative study Fye, Carol
1989
10 3 p. 337-
1 p.
artikel
99 Society for clinical trials board of directors, officers and committees 1989–1990 1989
10 3 p. 299-300
2 p.
artikel
100 Statistical analysis for studies with ordered hypothesis Fenwick, J.W.
1989
10 3 p. 346-
1 p.
artikel
101 Statistical considerations in the early termination of the multicenter trial of cryotherapy for retinopathy of prematurity 1989
10 3 p. 320-
1 p.
artikel
102 Statistical design of the treatment of mild hypertension study (TOMHS) Neaton, James D.
1989
10 3 p. 334-335
2 p.
artikel
103 Statistical methods for monitoring recruitment in a multicenter clinical trial Michele Melia, B.
1989
10 3 p. 345-
1 p.
artikel
104 Stochastic curtailment methods and confidence intervals 1989
10 3 p. 321-
1 p.
artikel
105 Tenth annual meeting of the Society for Clinical Trials 1989
10 3 p. 301-315
15 p.
artikel
106 The analysis of a crossover design with several replicates per subject Puterman, M.L.
1989
10 3 p. 348-
1 p.
artikel
107 The ASPIC trial: Telematics-assisted management of a multicenter clinical trial using a network of laptop personal computers Wurm, Michel
1989
10 3 p. 341-
1 p.
artikel
108 The clinical research management information system: An institutional database for tracking clinical trials Casper, Ephraim S.
1989
10 3 p. 342-
1 p.
artikel
109 The influence of a NIH funded study in a community hospital Bealer, Joan
1989
10 3 p. 352-
1 p.
artikel
110 The Mid-Atlantic Oncology Program's comparison of two data collection methods Jasperse, Dorcie M.
1989
10 3 p. 282-289
8 p.
artikel
111 The optimal use of a microcomputer system for distributed data entry Hartigan, Pamela
1989
10 3 p. 340-
1 p.
artikel
112 The pop-parent software system: A distributed data processing and clinical trial management system for the NHLBI BARI Amoroso, William P.
1989
10 3 p. 339-
1 p.
artikel
113 The problem of attributing deaths of nonadherers: The VA coronary bypass experience revisited 1989
10 3 p. 331-332
2 p.
artikel
114 The prophylactic penicillin (PROPS) trials 1989
10 3 p. 322-323
2 p.
artikel
115 The statistical component of Pfizer Pharmaceuticals PC-based Computer Assisted NDA (CANDA) system 1989
10 3 p. 326-
1 p.
artikel
116 The Studies of Left Ventricular Dysfunction (SOLVD) experience with a placebo run-phase 1989
10 3 p. 334-
1 p.
artikel
117 The use of factorial designs when the outcome variable is binary: What happens when low level interactions are present 1989
10 3 p. 323-324
2 p.
artikel
118 The use of registry as a complement to a clinical trial among patients with left-ventricular dysfunction (LVD) 1989
10 3 p. 325-
1 p.
artikel
119 The use of telemarketing techniques to enhance enrollment in clinical trials Butt, Rodney W.
1989
10 3 p. 352-353
2 p.
artikel
120 To stop or not to stop: A case study 1989
10 3 p. 321-
1 p.
artikel
121 Toxicity grading systems for oncological trials Franklin, H.R.
1989
10 3 p. 351-
1 p.
artikel
122 Training and certification of personnel in the asymptomatic carotid atherosclerosis study Howard, Virginia J.
1989
10 3 p. 344-
1 p.
artikel
123 Use of ejection fraction as a surrogate endpoint for death in clinical trials of acute myocardial infraction Harrelson, Lynn
1989
10 3 p. 349-
1 p.
artikel
124 Use of the triangular test in phase II cancer clinical trials 1989
10 3 p. 321-322
2 p.
artikel
125 Using a simple computer database to enhance clinic visit management Frost, Philip H.
1989
10 3 p. 342-
1 p.
artikel
126 Using efficiency calculations to choose between logrank and Cox model analyses 1989
10 3 p. 330-
1 p.
artikel
127 Vertebral fracture as an end-point for clinical trials in osteoporosis: The reliability of digitizing techniques for vertebral area measurements Tilley, B.C.
1989
10 3 p. 349-
1 p.
artikel
128 When to randomize? 1989
10 3 p. 324-
1 p.
artikel
                             128 gevonden resultaten
 
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