Related Experiment Video
Updated: May 26, 2026

In Silico Clinical Trials for Cardiovascular Disease
Published on: May 27, 2022
Secondary analysis of clinical trials--a cautionary note
1Division of Neurology Products, CDER, US Food & Drug Administration, Silver Spring, MD 20993-0002, USA. john.marler@fda.hhs.gov
Abstract:
There is concern in published reports and reviews that patients are being harmed or denied effective treatment by the use of questionable results from secondary analyses of data from clinical trials. A well-reported secondary analysis must make clear to the reader the uncertainty of the result--so clear, in fact, that it should be an obvious part of the conclusions that implementation should await confirmation as the primary outcome in an adequately powered trial. Those who write, review and publish these reports have a responsibility to ensure that reports accurately describe the sources of uncertainty, explain complex methods and their weaknesses with clarity, and convince readers to require better evidence before changing their practice.
Related Concept Videos
Clinical Trials
There are four phases in a clinical trial. A phase one...
Clinical Trials: Overview
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Hazard Ratio
For example, in a clinical trial evaluating a...
Bioavailability Study Design: Healthy Subjects Versus Patients
Preclinical Development: Overview
