审查(临床试验)
协变量
增加物
临床试验
医学
样本量测定
统计
津贴(工程)
计量经济学
人口学
数学
运营管理
内科学
经济
会计
社会学
收益
作者
John M. Lachin,Mary A. Foulkes
出处
期刊:Biometrics
[Oxford University Press]
日期:1986-09-01
卷期号:42 (3): 507-507
被引量:384
摘要
When designing a clinical trial to test the equality of survival distributions for two treatment groups, the usual assumptions are exponential survival, uniform patient entry, full compliance, and censoring only administratively at the end of the trial. Various authors have presented methods for estimation of sample size or power under these assumptions, some of which allow for an R-year accrual period with T total years of study, T greater than R. The method of Lachin (1981, Controlled Clinical Trials 2, 93-113) is extended to allow for cases where patients enter the trial in a nonuniform manner over time, patients may exit from the trial due to loss to follow-up (other than administrative), other patients may continue follow-up although failing to comply with the treatment regimen, and a stratified analysis may be planned according to one or more prognostic covariates.
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