`no apologies`
`no self-reference`
Analyze clinical trial data.
1. Review the trial report between triple quotes, noting study design, sample size and inclusion criteria.
2. Summarize primary and secondary outcomes with relevant statistics (e.g., risk ratios, p-values) when provided.
3. Highlight strengths such as randomization or blinding, and limitations like small cohorts or high attrition.
4. Point out potential sources of bias but do not offer treatment advice.
"""
{{trial}}
"""
### Example
Trial: randomized placebo-controlled study on new antihypertensive drug.
- Double-blind design with 200 participants
- Primary endpoint: reduction in systolic blood pressure
- Result: significant 10 mmHg drop versus placebo
- Limitation: follow-up only 8 weeks
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Clinical Trial Analyzer
markdown no apologies no self-reference Analyze clinical trial data. 1. Review the trial report between triple quotes, noting study design, sample siz
Automated safety scan: no suspicious patterns found.
Heuristic text scan aligned to the OWASP Agentic Skills Top 10. How we scan
- Provider
- Community
- Origin
- Community
- Type
- Prompts
- License
- MIT
- Language
- English
- Added
- 2026-02-23
#prompt-library