{"slug":"mohitagw15856-clinical-trial-protocol","source_name":"mohitagw15856/clinical-trial-protocol","name":"Mohitagw15856/Clinical Trial Protocol","description":"Draft a clinical trial protocol synopsis with the elements regulators and IRBs expect. Use when asked to write a clinical trial protocol, a study protocol synopsis, a trial design, or to structure endpoints/eligibility/statistics for an interventional study. Produces a structured protocol synopsis — objectives, design, population with eligibility, interventions, endpoints, statistics, and safety/ethics — for expert review. (For non-clinical/UX research, use research-protocol.)","version":1,"lift":{"pass_rate_delta_pts":50,"pass_rate_pct":68.2,"total_cases":22,"passed_cases":15,"tokens_delta_pct":40.8,"turns_delta_pct":0,"verdict":"mixed","benchmark_model":"gemini-3.6-flash","grading_method":"judged","completed_at":"2026-08-14T03:41:40.179450+00:00"},"skill_score":0.6818,"benchmark_models":[{"model":"gemini-3.6-flash","headline":true,"delta_pts":50,"with_pass_pct":68.2,"without_pass_pct":18.2,"tokens_delta_pct":40.8,"turns_delta_pct":0,"total_cases":22,"cases_aggregated":22,"verdict":"mixed","never_hurt":true,"completed_at":"2026-08-14T03:41:40.179450+00:00","run_id":"a208d0bb-860a-4130-9eef-0bda5c67cff2","version_number":1,"is_latest_version":true,"gate":null}],"trust":{"skill_safety":"passed","safety_status":"clean","intent_verdict":"safe","content_status":"clean","indexable":true},"license":"MIT","install_count":0,"manifest_hash":"6de8c5939dca75fedc203764fc2495f0c3d3a653f49eadc3d5f0cf031237d079","raw_url":"https://app.decimal.ai/s/mohitagw15856-clinical-trial-protocol/SKILL.md","scorecard_url":"https://app.decimal.ai/skills/mohitagw15856-clinical-trial-protocol"}