Glossary
Explore Our Glossary of Clinical Research Terms & Definitions.
Risk Assessment
The evaluation of potential risks and benefits to participants in a clinical trial.
Therapeutic Misconception
When participants incorrectly believe the trial�s purpose is to provide personal medical care.
Expanded Access Program
A way for patients to access investigational treatments outside clinical trials.
Minimal Risk
A level of harm or discomfort in a study that is no greater than that encountered in daily life.
Investigational Device Exemption (IDE)
FDA authorization to test a medical device in a clinical trial.
Conflict of Interest
Situations where personal or financial interests may influence clinical trial conduct.
Blinded Endpoint Evaluation
Ensuring that those assessing outcomes are unaware of group assignments.
Interim Analysis
An evaluation of trial data before the study is completed, often to ensure safety or efficacy.
Adaptive Trial Design
A flexible trial structure that allows for modifications based on interim results.
Data Analysis
The evaluation and interpretation of data collected during the clinical trial.
Screening Failure
A participant who does not meet eligibility criteria during the screening phase.
Good Clinical Practice (GCP)
Ethical and scientific standards for designing, conducting, and reporting clinical trials.
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