Clinical trials rarely, if ever, occur in a vacuum. Generally, large amounts of clinical data are available prior to the start of a study, particularly on the current study’s control arm. There is obvious appeal in using (i.e., ‘borrowing’) this information. With historical data providing information on the control arm, more trial resources can be devoted to the novel treatment while retaining accurate estimates of the current control arm parameters. This can result in more accurate point estimates, increased power, and reduced type I error in clinical trials, provided the historical information is sufficiently similar to the current control data. If this assumption of similarity is not satisfied, however, one can acquire increased mean squ...
Historical information is always relevant for designing clinical trials. The incorporation of histor...
In current clinical trial development, historical information is receiving more attention as it prov...
University of Minnesota Ph.D. dissertation. August 2010. Major: Biostatistics. Advisor: Bradley P. C...
Clinical trials rarely, if ever, occur in a vacuum. Generally, large amounts of clinical data are av...
BACKGROUND: While placebo-controlled randomised controlled trials remain the standard way to evaluat...
A standard two‐arm randomised controlled trial usually compares an intervention to a control treatme...
In order for historical data to be considered for inclusion in the design and analysis of clinical t...
Obstacles sometimes limit enrollment in randomized clinical trials of an exper- imental product vers...
The most common type of confirmatory trial is a randomised trial comparing the experimental treatmen...
Including historical data may increase the power of the analysis of a current clinical trial and red...
Data of previous trials with a similar setting are often available in the analysis of clinical trial...
Funder: National Institute of Health Research (NIHR) Cambridge Biomedical Research CentreA standard ...
High quality historical control data, if incorporated, may reduce sample size, trial cost and durati...
High quality historical control data, if incorporated, may reduce sample size, trial cost, and durat...
International audienceBACKGROUND:Performing well-powered randomised controlled trials (RCTs) of new ...
Historical information is always relevant for designing clinical trials. The incorporation of histor...
In current clinical trial development, historical information is receiving more attention as it prov...
University of Minnesota Ph.D. dissertation. August 2010. Major: Biostatistics. Advisor: Bradley P. C...
Clinical trials rarely, if ever, occur in a vacuum. Generally, large amounts of clinical data are av...
BACKGROUND: While placebo-controlled randomised controlled trials remain the standard way to evaluat...
A standard two‐arm randomised controlled trial usually compares an intervention to a control treatme...
In order for historical data to be considered for inclusion in the design and analysis of clinical t...
Obstacles sometimes limit enrollment in randomized clinical trials of an exper- imental product vers...
The most common type of confirmatory trial is a randomised trial comparing the experimental treatmen...
Including historical data may increase the power of the analysis of a current clinical trial and red...
Data of previous trials with a similar setting are often available in the analysis of clinical trial...
Funder: National Institute of Health Research (NIHR) Cambridge Biomedical Research CentreA standard ...
High quality historical control data, if incorporated, may reduce sample size, trial cost and durati...
High quality historical control data, if incorporated, may reduce sample size, trial cost, and durat...
International audienceBACKGROUND:Performing well-powered randomised controlled trials (RCTs) of new ...
Historical information is always relevant for designing clinical trials. The incorporation of histor...
In current clinical trial development, historical information is receiving more attention as it prov...
University of Minnesota Ph.D. dissertation. August 2010. Major: Biostatistics. Advisor: Bradley P. C...