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A comparison of methods for designing hybrid type 2 cluster-randomized trials with continuous effectiveness and implementation endpoints
Arxiv
0+阅读 · 5月14日
PWEXP: An R Package Using Piecewise Exponential Model for Study Design and Event/Timeline Prediction
Arxiv
0+阅读 · 5月12日
Q-approximation of operating characteristics of clinical trial designs
Arxiv
0+阅读 · 3月20日
A Multi-Stage Drop-the-Loser Design with Superiority Boundaries
Arxiv
0+阅读 · 4月10日
On the inclusion of non-concurrent controls in platform trials with an interim analysis
Arxiv
0+阅读 · 3月24日
Is control of type I error rate needed in Bayesian clinical trial designs?
Arxiv
0+阅读 · 3月24日
Sample size calculations for multilevel factorial longitudinal cluster randomised trials
Arxiv
0+阅读 · 5月1日
Accounting for Heavy Censoring in Evaluating the Risk Stratification Abilities of Existing Models for Time to Diagnosis of Huntington Disease
Arxiv
0+阅读 · 3月14日
Designing clinical trials for the comparison of single and multiple quantiles with right-censored data
Arxiv
0+阅读 · 3月9日
Designing clinical trials for the comparison of single and multiple quantiles with right-censored data
Arxiv
0+阅读 · 3月6日
Bayesian Design and Analysis of Precision Trials with Partial Borrowing
Arxiv
0+阅读 · 3月11日
Some Bayesian Perspectives on Clinical Trials
Arxiv
0+阅读 · 2月9日
Learning from Literature: Integrating LLMs and Bayesian Hierarchical Modeling for Oncology Trial Design
Arxiv
0+阅读 · 2月9日
An Adaptive Phase II Trial Design for Dose Selection and Addition in Microfilarial Infections
Arxiv
0+阅读 · 1月20日
A response-adaptive multi-arm design for continuous endpoints based on a weighted information measure
Arxiv
0+阅读 · 1月15日
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