ClinicalTrials pdf

Author: Curtis L. Meinert
Edition: 2
Publisher: Oxford University Press, USA
Binding: Hardcover
ISBN: 0195387880

ClinicalTrials: Design, Conduct and Analysis (Monographs in Epidemiology and Biostatistics)

First published in 1986, this landmark text is the definitive guide to clinical trials, written by one of the leading experts in the field. Medical books ClinicalTrials. This fully-updated second edition continues to be the most authoritative reference text on randomized clinical trials. It contains a wealth of practical information on the design, conduct, and analysis of both single center and multicenter trials. No other book on clinical trials offers as much detail on such issues as sample size calculation, stratification and randomization, data systems design, development of consent forms, publication policies, preparation of funding requests, and reporting procedures.

While the basics of design, conduct, and analysis of clinical trials remain the same, there have been significant changes since the first edition of Clinical Trials was published two decades ago Medical books Developing a National Registry of Pharmacologic and Biologic Clinical Trials: Workshop Report. Categories: Clinical trials, Registries. Contributors: Committee on Clinical Trial Registries - Author. Format: Paperback

Download link for Multi-Center Phase III Clinical Trials and NCI Cooperative Groups: Workshop Summary

Categories: Clinical trials, Registries. Contributors: Committee on Clinical Trial Registries - Author. Format: Paperback

This edition includes both updates and new uses and issues concerning CTS, along with case studies of how clinical trial simulations are being applied in various therapeutic and application areas. Importantly, the book expands on the utility of CTS for informing decisions during drug development and regulatory review. Each chapter author was selected on the basis of demonstrated expertise in state-of-the-art application of CTS.
The target audience for this volume includes researchers and scientists who wish to consider use of simulations in the design, analysis, or regulatory review and guidan

Categories: Outcome Assessment (Health Care), Clinical trials, Outcome assessment (Medical care). Contributors: Stephen J. Walters - Author. Format: Hardcover

Medical Book ClinicalTrials

This fully-updated second edition continues to be the most authoritative reference text on randomized clinical trials. It contains a wealth of practical information on the design, conduct, and analysis of both single center and multicenter trials. No other book on clinical trials offers as much detail on such issues as sample size calculation, stratification and randomization, data systems design, development of consent forms, publication policies, preparation of funding requests, and reporting procedures.

While the basics of design, conduct, and analysis of clinical trials remain the same, there have been significant changes since the first edition of Clinical Trials was published two decades ago. In this new edition, the author discusses the refinements and improvements made to methods and procedures, changes in the policies and guidelines underlying trials, as well as requirements for registration of trials. He also discusses current practices for data sharing, for gender representation, for treatment effects monitoring, and for ethical standards of clinical trials. The importance of the randomized controlled trial has grown significantly over time and they are now the cornerstone of all evidence-based medicine. Still rich in tables, checklists, charts, and other resources for the trialist, the second edition of Clinical Trials is an indispensable reference for clinicians, biostaticians, epidemiologists, and anyone involved in the design and implementation of a clinical trial.