BACKGROUND AND OBJECTIVE: Prespecification of statistical methods in clinical trial protocols and statistical analysis plans can help to deter bias from p-hacking but is only effective if the prespecified approach is made available. STUDY DESIGN AND SETTING: For 100 randomized trials published in 2018 and indexed in PubMed, we evaluated how often a prespecified statistical analysis approach for the trial's primary outcome was publicly available. For each trial with an available prespecified analysis, we compared this with the trial publication to identify whether there were unexplained discrepancies. RESULTS: Only 12 of 100 trials (12%) had a publicly available prespecified analysis approach for their primary outcome; this document was date...
Preregistration entails researchers registering their planned research hypotheses, methods, and anal...
OBJECTIVE: To examine the extent and nature of outcome reporting bias in a broad cohort of published...
Transparency and reproducibility are two of the fundamental principles of evidence generation and di...
OBJECTIVE: Pre-specification of statistical methods in clinical trial protocols and Statistical Anal...
BACKGROUND: Choosing or altering the planned statistical analysis approach after examination of tria...
Evidence of unexplained discrepancies between planned and conducted statistical analyses: a review o...
BACKGROUND: Access to protocols and statistical analysis plans (SAPs) increases the transparency of ...
Results from clinical trials can be susceptible to bias if investigators choose their analysis appro...
International audienceBackground: Protocols are often unavailable to peer-reviewers and readers. To ...
Background: All clinical research benefits from transparency and validity. Transparency and validity...
Clinical trials play a decisive role in the drug approval processes. By completing a p-curve analysi...
Objective To examine how poor reporting and inadequate methods for key methodological features in ra...
BACKGROUND: The analysis of clinical trials with dropout usually assumes the missing data are ;missi...
OBJECTIVE: To evaluate how often sample size calculations and methods of statistical analysis are pr...
UA Open Access Publishing FundBackground Missing outcome data is a threat to the validity of treatme...
Preregistration entails researchers registering their planned research hypotheses, methods, and anal...
OBJECTIVE: To examine the extent and nature of outcome reporting bias in a broad cohort of published...
Transparency and reproducibility are two of the fundamental principles of evidence generation and di...
OBJECTIVE: Pre-specification of statistical methods in clinical trial protocols and Statistical Anal...
BACKGROUND: Choosing or altering the planned statistical analysis approach after examination of tria...
Evidence of unexplained discrepancies between planned and conducted statistical analyses: a review o...
BACKGROUND: Access to protocols and statistical analysis plans (SAPs) increases the transparency of ...
Results from clinical trials can be susceptible to bias if investigators choose their analysis appro...
International audienceBackground: Protocols are often unavailable to peer-reviewers and readers. To ...
Background: All clinical research benefits from transparency and validity. Transparency and validity...
Clinical trials play a decisive role in the drug approval processes. By completing a p-curve analysi...
Objective To examine how poor reporting and inadequate methods for key methodological features in ra...
BACKGROUND: The analysis of clinical trials with dropout usually assumes the missing data are ;missi...
OBJECTIVE: To evaluate how often sample size calculations and methods of statistical analysis are pr...
UA Open Access Publishing FundBackground Missing outcome data is a threat to the validity of treatme...
Preregistration entails researchers registering their planned research hypotheses, methods, and anal...
OBJECTIVE: To examine the extent and nature of outcome reporting bias in a broad cohort of published...
Transparency and reproducibility are two of the fundamental principles of evidence generation and di...