Designing a longitudinal clinical trial based on a composite endpoint: sample size, monitoring, and adaptation
From MaRDI portal
Publication:6629323
DOI10.1002/SIM.9416zbMATH Open1547.62445MaRDI QIDQ6629323FDOQ6629323
Authors: David A. Schoenfeld, Ritesh Ramchandani, Dianne M. Finkelstein 
Publication date: 29 October 2024
Published in: Statistics in Medicine (Search for Journal in Brave)
Cites Work
- An alternative approach to confidence interval estimation for the win ratio statistic
- Title not available (Why is that?)
- A simple algorithm for designing group sequential clinical trials
- On the win-ratio statistic in clinical trials with multiple types of event
- On the inefficiency of the adaptive design for monitoring clinical trials
- Adaptive design theory and implementation using SAS and R.
- Graphing the win ratio and its components over time
This page was built for publication: Designing a longitudinal clinical trial based on a composite endpoint: sample size, monitoring, and adaptation
Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q6629323)
