{
  "value": "clinical_trial_protocol_summary",
  "label": "Summarize Clinical Trial Protocols",
  "description": "This workflow creates clear summaries of complex clinical trial protocols. Paste the detailed protocol including inclusion/exclusion criteria, study design, endpoints, and procedures, and the AI will generate concise summaries suitable for different audiences like investigators, ethics committees, or sponsors.",
  "name": "Protocol Summary",
  "category": "Pharmaceuticals",
  "type": "Industry",
  "config": {
    "temperature": 10,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Create a clear and structured summary of this clinical trial protocol. Include the study objective, design (phase, randomization, blinding), key inclusion/exclusion criteria, primary and secondary endpoints, treatment arms with dosing, main procedures and visit schedule, and sample size. Organize with clear headings and bullet points. Keep medical terminology but explain complex concepts briefly. Focus on what investigators and staff need to know to run the trial properly."
      }
    ]
  }
}