Inclusion/exclusion criteria for trial participation.

NIAID Data Ecosystem2026-05-01 收录

临床试验设计

受试者筛选

数据链接：

https://figshare.com/articles/dataset/Inclusion_exclusion_criteria_for_trial_participation_/24111125 数据链接链接失效反馈

官方服务：

资源简介：

Inclusion/exclusion criteria for trial participation.

创建时间：

2023-09-08

Sensitivity Analyses of Clinical Trial Designs: Selecting Scenarios and Summarizing Operating Characteristics

临床试验设计

敏感性分析

The use of simulation-based sensitivity analyses is fundamental for evaluating and comparing candidate designs of future clinical trials. In this context, sensitivity analyses are especially useful to

DataCite Commons2024-06-09 更新120

Design and progress status of the 11 PrEP trials appraised.

HIV预防

临床试验设计

Legend: Registration code: as per the National Institute of Health trials registry. Pill(s) tested: FTC = emtricitabine; TDF = tenofovir.

NIAID Data Ecosystem40

Resources for Biostatistics paper "Bayesian Clinical Trial Design Using Historical Data that Inform the Treatment Effect" by Psioda and Ibrahim.

贝叶斯统计

临床试验设计

This zipped tar ball contains all the files (programs, data sets, program logs, shell scripts for cluster computing, etc.) that were used to produce the results in the paper referenced in the title.

DataCite Commons2020-08-31 更新30

Treatment Selection at Interim Analysis Based on a Correlated Early Endpoint in Adaptive Two-Stage Trials with a Primary Endpoint Based on Count Data

临床试验设计

统计

Adaptive two-stage design with treatment selection, also called seamless Phase II/III design, has been recognized to save sample size and time to enhance the development of effective treatments. These

Taylor & Francis Group2025-07-29 更新40

Sample size calculations for superiority trials.

临床试验设计

样本量计算

Efficacy in the reference arm from 60–80%, delta 10–30%, alpha error 0.05, power 80–95%.

Figshare2015-12-02 更新30