clinical-trials
CommunityClear, actionable clinical trial interpretation.
Education & Research#bias#interpretation#effect-size#consort#clinical-trial#confidence-interval#clinical-relevance
Authorry86pkqf74-rgb
Version1.0.0
Installs0
System Documentation
What problem does it solve?
Interpreting clinical trial results is challenging and requires structured guidance to evaluate effect sizes, precision, bias, and reporting quality.
Core Features & Use Cases
- Standardizes interpretation of primary and secondary outcomes (HR, OR, RR, ARR, NNT/NNH) with clinical context.
- Applies CONSORT 2010 guidelines to assess reporting quality, risk of bias, and generalizability across trial designs (RCTs, non-inferiority, adaptive, observational).
- Highlights common pitfalls (surrogate endpoints, non-pre-specified subgroups, sponsor bias) and provides corrective phrasing templates.
Quick Start
Interpret a trial report focusing on HR 0.75 (CI 0.60–0.93) and ARR 5%, and explain the clinical relevance and needed follow-up.
Dependency Matrix
Required Modules
None requiredComponents
Standard package💻 Claude Code Installation
Recommended: Let Claude install automatically. Simply copy and paste the text below to Claude Code.
Please help me install this Skill: Name: clinical-trials Download link: https://github.com/ry86pkqf74-rgb/ROS_FLOW_2_1/archive/main.zip#clinical-trials Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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