Home - Tagged as 'clinical trial'

Fast tracking informative clinical trials: lessons for mental health

The 5 Principles To Guide The Future Of Randomized Clinical Trials

Enabling "Good" Clinical Research In LMICs With The Good Clinical Trials Collaborative

Guidelines for the Content of Statistical Analysis Plans in Clinical Trials

While guidance on statistical principles for clinical trials exists, there is an absence of guidance covering the required content of statistical analysis plans (SAPs) to support transparency and reproducibility. Recommendations are provided for a minimum set of items that should be addressed and included in SAPs for clinical trials. Trial registration, protocols, and statistical analysis plans are critically important in ensuring appropriate reporting of clinical trials.

Development of an online resource for recruitment research in clinical trials to organise and map current literature

Transparency in the conduct and reporting of clinical trials is supported by the guidance produced on the content of clinical trial protocols and reporting standards for clinical trials. While the principle features of the statistical analysis are required within this guidance it is generally accepted that a separate Statistical Analysis Plan is also developed as the level of detail appropriate for a SAP is excessive for a protocol. However, there is no detailed guidance on the content of a SAP and consequently, there is marked variation in practice. 

Guidelines for Clinical Trial Registration

An overview on trial registration. Here you can find out why trials need to be registered and what the difference is between all the registries - and how to register your study.