Biostatistics in clinical trials /

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Bibliographic Details
Imprint:Chichester [England] ; New York : J. Wiley, c2001.
Description:xx, 501 p. : ill. ; 26 cm.
Language:English
Series:The Wiley reference series in biostatistics
Wiley reference series in biostatistics.
Subject:
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/4424163
Hidden Bibliographic Details
Other authors / contributors:Redmond, Carol K.
Colton, Theodore.
ISBN:0471822116 (alk. paper)
Notes:Includes bibliographical references and index.

MARC

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505 0 0 |t Adaptive and Dynamic Methods of Treatment Assignment --  |t Antibacterial Agent Trials --  |t Audit and Quality Control --  |t Bayesian Methods --  |t Benefit/Risk Assessment --  |t Blinding or Masking --  |t Clinical Significance Versus Statistical Significance --  |t Clinical Trials, Overview --  |t Cluster Randomization --  |t Cochrane Collaboration --  |t Community Intervention Trials --  |t Compliance Assessment --  |t Consort --  |t Controlled Clinical Trials --  |t Cooperative Cancer Trials --  |t Cooperative Heart Disease Trials --  |t Cooperative Studies Program, US Department of Veterans Affairs --  |t Cost-effectiveness --  |t Covariate Imbalance, Adjustment for --  |t Crossover Designs --  |t Data and Safety Monitoring --  |t Data and Safety Monitoring Boards --  |t Data Management and Coordination --  |t Drug Approval and Regulation --  |t Drug Interaction --  |t Eligibility and Exclusion Criteria --  |t Equivalence Trials --  |t Ethics --  |t European Federation of Statisticians in the Pharmaceutical Industry (EFSPI) --  |t European Organization for Research and Treatment of Cancer (EORTC) --  |t Factorial Designs --  |t Fraud --  |t Group-randomization Designs --  |t Guidelines --  |t Historical Controls, Bias From --  |t History, Early Cancer and Heart Disease Trials --  |t History, Overview --  |t Intention-to-Treat Analysis --  |t International Studies of Infarct Survival (ISIS) --  |t Medical Ethics and Statistics --  |t Medical Research Council (MRC) Streptomycin Trial --  |t Meta-analysis --  |t Missing Data --  |t Multicenter Trials --  |t Multiple Endpoints --  |t Multiplicity --  |t Noncompliance, Adjustment for --  |t Nonrandomized Trials --  |t NSABP and Advances in the Treatment of Breast Cancer --  |t Number Needed to Treat (NNT) --  |t Outcome Measures --  |t Pharmaceutical Industry, Statistics in --  |t Phase I Trials --  |t Phase II Trials --  |t Physicians' Health Study --  |t Postmarketing Surveillance of New Drugs and Assessment of Risk --  |t Preclinical Treatment Evaluation --  |t Prevention Trials --  |t Protocols --  |t QUOROM --  |t Randomization --  |t Randomized Treatment Assignment --  |t Salk Vaccine --  |t Sample Size Determination --  |t Screening Trials --  |t Sequential Methods --  |t Society for Clinical Trials --  |t Software --  |t Statistical Review for Medical Journals --  |t Statistical Review for Medical Journals, Guidelines for Authors --  |t Statisticians in the Pharmaceutical Industry (SPI) --  |t Surrogate Endpoints --  |t Textbooks --  |t Time-varying Treatment Effect --  |t Treatment-Covariate Interaction --  |t University Group Diabetes Program (UGDP) --  |t Vaccine Studies. 
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