Planning and evaluating clinical trials with composite time-to-first-event endpoints in a competing risk framework-Reference-Cited by-同舟云学术

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Planning and evaluating clinical trials with composite time-to-first-event endpoints in a competing risk framework

Published:2013-04-02 Issue:21 Volume:32 Page:3595-3608
ISSN:0277-6715
Container-title:Statistics in Medicine
language:en
Short-container-title:Statist. Med.

Author:

Rauch G.¹,Beyersmann J.²³

Affiliation:

1. Institute of Medical Biometry and Informatics; University of Heidelberg; Im Neuenheimer Feld 305 69120 Heidelberg Germany

2. Institute of Medical Biometry and Medical Informatics; University Medical Center Freiburg; Stefan-Meier-Str. 26 79104 Freiburg Germany

3. Freiburg Center for Data Analysis and Modeling; University of Freiburg; Eckerstr. 1 79104 Freiburg Germany

Publisher

Wiley

Subject

Statistics and Probability,Epidemiology

Reference50 articles.

1. Survival end point reporting in randomized cancer clinical trials: a review of major journals;Mathoulin-Pelissier;Journal of Clinical Oncology,2008

2. Composite outcomes in cardiovascular research: a survey of randomized trials;Lim;Annals of Internal Medicine,2008

3. Problems with the use of composite end points in cardiovascular trials: systematic review of randomised controlled trials;Ferreira-Gonzàles;British Medical Journal,2007

4. Composite endpoints for clinical trials: current perspectives;Kleist;International Journal of Pharmaceutical Medicine,2007

5. Combined endpoints: can we use them?;Lubsen;Statistics in Medicine,2002

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