Generate clinical trial protocols for medical devices or drugs. This skill should be used when users say "Create a clinical trial protocol", "Generate protocol for [device/drug]", "Help me design a clinical study", "Research similar trials for [intervention]", or when developing FDA submission documentation for investigational products.
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Generate clinical trial protocols for medical devices or drugs. This skill should be used when users say "Create a clinical trial protocol", "Generate protocol for [device/drug]", "Help me design a clinical study", "Research similar trials for [intervention]", or when developing FDA submission documentation for investigational products.
Clinical Trial Protocol Skill
⚠️ EXECUTION CONTROL - READ THIS FIRST
CRITICAL: This orchestrator follows a SIMPLE START approach:
Display the welcome message FIRST (shown in "Startup: Welcome and Confirmation" section below)
Ask user to confirm they're ready to proceed - Wait for confirmation (yes/no)
Jump directly into Full Workflow Logic - Automatically run subskills sequentially
Do NOT pre-read subskill files - Subskills are loaded on-demand only when their step executes
Why this matters:
Pre-reading all subskills wastes context and memory
Subskills should only load when actually needed during execution
Workflow automatically handles resuming from existing waypoints
Overview
This skill generates clinical trial protocols for medical devices or drugs using a modular, waypoint-based architecture
What This Skill Does
Starting with an intervention idea (device or drug), this orchestrated workflow offers two modes:
🔬 Research Only Mode (Steps 0-1):
0. Initialize Intervention - Collect device or drug information
Research Similar Protocols - Find similar trials, FDA guidance, and published protocols
Deliverable: Comprehensive research summary as formatted .md artifact
📄 Full Protocol Mode (Steps 0-5):
0. Initialize Intervention - Collect device or drug information
Research Similar Protocols - Find similar trials, FDA guidance, and published protocols
Protocol Foundation - Generate protocol sections 1-6 (foundation, design, population)
Rich Initial Context Support:
Users can provide substantial documentation, technical specifications, or research data when initializing the intervention (Step 0). This is preserved in intervention_metadata.json under the initial_context field. Later steps reference this context for more informed protocol development.
Modular Subskill Steps
Each step is an independent skill in references/ directory:
references/
├── 00-initialize-intervention.md # Collect device or drug information
├── 01-research-protocols.md # Clinical trials research and FDA guidance
├── 02-protocol-foundation.md # Protocol sections 1-6 (foundation, design, population)
├── 03-protocol-intervention.md # Protocol sections 7-8 (intervention details)
├── 04-protocol-operations.md # Protocol sections 9-12 (assessments, statistics, operations)
└── 05-generate-document.md # NIH Protocol generation
Utility Scripts
scripts/
└── sample_size_calculator.py # Statistical power analysis (validated)
Prerequisites
1. clinical trials MCP Server (Required)
Installation:
Install via drag-and-drop .mcpb file into Claude Desktop
Or configure manually in Claude Desktop settings
Available Tools:search_clinical_trials - Search by:
condition - Disease or condition (e.g., "pancreatic cancer")
intervention - Drug, device, or treatment (e.g., "pembrolizumab", "CAR-T")
sponsor - Sponsor or collaborator name (e.g., "Pfizer", "NIH")
location - City, state, or country (e.g., "California", "Boston")
status - "recruiting" (default), "active", "completed", "all"
phase - Trial phase: "1", "2", "3", "4", "early_phase1"
max_results - Default 25, max 100
get_trial_details - Get comprehensive details for a specific trial using its nct_id (e.g., "NCT04267848"). Returns eligibility criteria, outcomes, study design, and contact information.
Verification: Step 1 will automatically test MCP connectivity at startup.
2. FDA Database Access (Built-in)
Purpose: FDA regulatory pathway research via explicit database URLs
Sources:
Step 1: FDA device/drug databases (510(k), PMA, De Novo, Drugs@FDA, Orange Book, Purple Book)
All sources use direct FDA database URLs - no generic web searches
3. Clinical Protocol Template
Template Files: Any .md files in the assets/ directory
Purpose: Reference template for protocol structure and content guidance. The system automatically detects available templates and uses them dynamically.
4. Python Dependencies (Required for Step 2)
Installation:
pip install -r requirements.txt
Dependencies:
scipy >= 1.11.0 (statistical calculations)
numpy >= 1.24.0 (numerical operations)
Purpose: Accurate statistical sample size calculations for clinical protocols
How to Use
Simply invoke the skill and select your desired mode:
🔬 Research Only Mode:
Select "Research Only" from the main menu
Provide intervention information
Receive comprehensive research summary as formatted .md artifact
Option to continue with full protocol generation or exit
📄 Full Protocol Mode:
Select "Full Protocol" from the main menu
Guide you through all steps sequentially (Steps 0-5)
Pause after Step 4 to review the draft protocol
Generate the final protocol document when ready
Resume Capability: If interrupted, simply restart the skill and it will automatically resume from your last completed step.
Execution Flow
Startup: Welcome and Mode Selection
When skill is invoked, display the following message:
🧬 CLINICAL TRIAL PROTOCOL
Welcome! This skill generates clinical trial protocols for medical devices or drugs.
[If waypoints/intervention_metadata.json exists:]
✓ Found existing protocol in progress: [Intervention Name]
Type: [Device/Drug]
Completed: [List of completed steps]
Next: [Next step to execute]
📋 SELECT MODE:
1. 🔬 Research Only - Run clinical research analysis (Steps 0-1)
• Collect intervention information
• Research similar clinical trials
• Find FDA guidance and regulatory pathways
• Generate comprehensive research summary as .md artifact
2. 📄 Full Protocol - Generate complete clinical trial protocol (Steps 0-5)
• Everything in Research Only, plus:
• Generate all protocol sections
• Create professional protocol document
3. ❌ Exit
Please select an option (1, 2, or 3):
🛑 STOP and WAIT for user selection (1, 2, or 3)
If 1 (Research Only): Set execution_mode = "research_only" and proceed to Research Only Workflow Logic
If 2 (Full Protocol): Set execution_mode = "full_protocol" and proceed to Full Workflow Logic
If 3 (Exit): Exit gracefully with "No problem! Restart the skill anytime to continue."
Research Only Workflow Logic
This workflow executes only Steps 0 and 1, then generates a formatted research summary artifact.
Step 1: Check for Existing Waypoints
If waypoints/intervention_metadata.json exists: Load metadata, check if steps 0 and 1 are already complete
If no metadata exists: Start from Step 0
Step 2: Execute Research Steps (0 and 1)
For each step (0, 1):
Check completion status: If step already completed in metadata, skip with "✓ Step [X] already complete"
Execute step:
Display "▶ Executing Step [X]..."
Read and follow the corresponding subskill file instructions
Wait for completion
Display "✓ Step [X] complete"
Step execution method (ON-DEMAND LOADING): When a step is ready to execute (NOT before), read the subskill markdown file and execute ALL instructions within it
Create formatted markdown summary: Generate a comprehensive, well-formatted research summary as a markdown artifact with the following structure:
# Clinical Research Summary: [Intervention Name]## Intervention Overview-**Type:** [Device/Drug]
-**Indication:** [Target condition/disease]
-**Description:** [Brief intervention description]
-**Mechanism of Action:** [How it works]
## Similar Clinical Trials
[List top 5-10 similar trials with NCT ID, title, phase, status, key findings]
## FDA Regulatory Pathway-**Recommended Pathway:** [510(k), PMA, De Novo, IND, NDA, BLA, etc.]
-**Regulatory Basis:** [Rationale for pathway selection]
-**Key Requirements:** [Major regulatory considerations]
## FDA Guidance Documents
[List relevant FDA guidance documents with links and key excerpts]
## Study Design Recommendations-**Suggested Study Type:** [RCT, single-arm, etc.]
-**Phase Recommendation:** [Phase 1, 2, 3, etc.]
-**Primary Endpoint Suggestions:** [Based on similar trials]
-**Sample Size Considerations:** [Preliminary thoughts]
## Key Insights and Recommendations
[Synthesized recommendations for protocol development]
## Next Steps
[If user wants to proceed with full protocol development]
---
*Generated by Clinical Trial Protocol Skill**Date: [Current date]*
Save artifact: Write the formatted summary to waypoints/research_summary.md
Display completion message:
✅ RESEARCH COMPLETE
Research Summary Generated: waypoints/research_summary.md
📊 Key Findings:
• Similar Trials Found: [X trials]
• Recommended Pathway: [Pathway name]
• FDA Guidance Documents: [X documents identified]
• Study Design: [Recommended design]
📄 The research summary has been saved as a formatted markdown artifact.
Would you like to:
1. Continue with full protocol generation (steps 2-5)
2. Exit and review research summary
Option 1 Logic (Continue to Full Protocol):
Set execution_mode = "full_protocol"
Continue to Full Workflow Logic starting from Step 2 (since 0 and 1 are complete)
Option 2 Logic (Exit):
Display: "✓ Research summary saved. Restart the skill anytime to continue with protocol generation."
Exit orchestrator gracefully
Full Workflow Logic
Step 1: Check for Existing Waypoints
If waypoints/intervention_metadata.json exists: Load metadata, check completed_steps array, resume from next incomplete step
If no metadata exists: Start from Step 0
Step 2: Execute Steps in Order
For each step (0, 1, 2, 3, 4, 5):
Check completion status: If step already completed in metadata, skip with "✓ Step [X] already complete"
Execute step: Display "▶ Executing Step [X]...", read and follow the corresponding subskill file instructions, wait for completion, display "✓ Step [X] complete"
Step execution method (ON-DEMAND LOADING): When a step is ready to execute (NOT before), read the subskill markdown file and execute ALL instructions within it
IMPORTANT: Do NOT read subskill files in advance. Only read them at the moment of execution.
Step-to-file mapping:
Step 0: references/00-initialize-intervention.md (read when Step 0 executes)
Step 1: references/01-research-protocols.md (read when Step 1 executes)
Step 5: references/05-concatenate-protocol.md (read when Step 5 executes - final concatenation)
Handle errors: If step fails, ask user to retry or exit. Save current state for resume capability.
Display progress: "Progress: [X/6] steps complete", show estimated remaining time
Step 4 Completion Pause: After Step 4 completes, pause and display the Protocol Completion Menu (see below). Wait for user selection before proceeding.
Step 2.5: Protocol Completion Menu
After Step 4 completes successfully, display the EXACT menu below (do not improvise or create alternative options):
✅ PROTOCOL COMPLETE: Protocol Draft Generated
Protocol Details:
• Study Design: [Design from metadata]
• Sample Size: [N subjects from metadata]
• Primary Endpoint: [Endpoint from metadata]
• Study Duration: [Duration from metadata]
Protocol file: waypoints/02_protocol_draft.md
File size: [Size in KB]
📋 WHAT WOULD YOU LIKE TO DO NEXT?
1. 📄 Review Protocol in Artifact - click on the .md file above
2. 📄 Concatenate Final Protocol (Step 5)
3. ⏸️ Exit and Review Later
Option 1 Logic (Review in Artifact):
Pause, let user open the section files, wait for further instruction
Option 2 Logic (Concatenate Protocol):
Execute Step 5 by reading and following references/05-concatenate-protocol.md
Step 5 will concatenate all section files into final protocol document
Continue to Step 3 (Final Summary) after Step 5 completes
Option 3 Logic (Exit):
Display: "✓ Protocol sections saved. You can resume with Step 5 anytime to concatenate."
Individual section files preserved for easier regeneration
Data Minimization Strategy
Each step implements aggressive summarization:
Keep: Top-N results (5-10 max)
Keep: Key facts and IDs (NCT numbers, endpoint types)
Keep: Concise rationale (2-3 sentences)
Discard: Raw MCP query results (not needed after analysis)
Discard: Full FDA guidance text (only excerpts/citations kept)
Discard: Lower-ranked search results
Step Independence
Each subskill is designed to:
Read only from waypoint files (not conversation history)
Produce complete output in single execution
Not depend on conversation context from previous steps
Be runnable standalone
Error Handling
MCP Server Unavailable
Detected in: Step 1
Action: Display error with installation instructions
Allow user to retry after installing MCP server
No fallback available - MCP server is required for protocol research
Step Fails or Returns Error
Action: Display error message from subskill
Ask user: "Retry step? (Yes/No)"
Yes: Re-run step
No: Save current state, exit orchestrator
User Interruption
All progress saved in waypoint files
User can resume anytime by restarting the skill
Workflow automatically detects completed steps and resumes from next step
No data loss
Disclaimers
⚠️ IMPORTANT: This protocol generation tool provides preliminary clinical study protocol based on NIH/FDA guidelines and similar trials. It does NOT constitute:
Official FDA or IRB determination or approval
Medical, legal, or regulatory advice
Substitute for professional biostatistician review
Substitute for FDA Pre-Submission meeting
Guarantee of regulatory or clinical success
REQUIRED before proceeding with clinical study:
Biostatistician review and sample size validation
FDA Pre-Submission meeting (Q-Submission for devices, Pre-IND for drugs)
IRB review and approval
Clinical expert and regulatory consultant engagement
Legal review of protocol and informed consent
Site investigator review and input
Sponsor completion of all [TBD] items in protocol
PROFESSIONAL CONSULTATION STRONGLY RECOMMENDED
Clinical trial protocols are complex, high-stakes documents requiring expertise across multiple disciplines. Professional consultation with clinical trial experts, biostatisticians, and regulatory affairs specialists is essential before proceeding with clinical study planning.
Implementation Requirements
When this skill is invoked:
Display the welcome message with mode selection (shown in "Startup: Welcome and Mode Selection" section)
Wait for user mode selection (1: Research Only, 2: Full Protocol, 3: Exit)
Execute based on selected mode:
Research Only Mode (Option 1):
Execute Research Only Workflow Logic (Steps 0-1 only)
Generate formatted research summary as .md artifact
Offer option to continue with full protocol or exit
Full Protocol Mode (Option 2):
Execute Full Workflow Logic (Steps 0-5)
Check for existing waypoints and resume from last completed step
OR start from Step 0 if no waypoints exist
Execute all steps sequentially until complete
For each step execution (LAZY LOADING - On-Demand Only):
ONLY when a step is ready to execute, read the corresponding subskill file
Do NOT read subskill files in advance or "to prepare"
Example: When Step 1 needs to run, THEN read references/01-research-protocols.md and follow its instructions
For protocol development: Execute Steps 2, 3, 4 sequentially in order
Do NOT try to execute multiple steps in parallel - run sequentially
Read each step's subskill file only when that specific step is about to execute
Research summary artifact generation (Research Only Mode):
