Clinical Trial Protocol Skill

🏢Official
by anthropics · vlatest · Repository

This skill extracts key details from clinical trial protocols to quickly understand study design and eligibility criteria – boosting research efficiency.

Install on your platform

We auto-selected Claude Code based on this skill’s supported platforms.

1

Run in terminal (recommended)

terminal
claude mcp add anthropics-clinical-trial-protocol-skill npx -- -y @trustedskills/anthropics-clinical-trial-protocol-skill
2

Or manually add to ~/.claude/settings.json

~/.claude/settings.json
{
  "mcpServers": {
    "anthropics-clinical-trial-protocol-skill": {
      "command": "npx",
      "args": [
        "-y",
        "@trustedskills/anthropics-clinical-trial-protocol-skill"
      ]
    }
  }
}

Requires Claude Code (claude CLI). Run claude --version to verify your install.

About This Skill

What it does

This skill allows AI agents to understand, analyze, and generate clinical trial protocols. It can extract key information from existing protocols, identify potential issues or inconsistencies, and draft new protocol sections based on provided requirements. The tool aims to streamline the often complex and time-consuming process of clinical trial development.

When to use it

  • Protocol Review: Quickly assess a draft protocol for completeness and adherence to regulatory guidelines.
  • Section Generation: Generate specific sections of a clinical trial protocol, such as inclusion/exclusion criteria or statistical analysis plans.
  • Data Extraction: Extract key data points (e.g., sample size, endpoints) from existing protocols for comparison or reporting.
  • Consistency Checks: Identify inconsistencies between different parts of a protocol to ensure accuracy and clarity.

Key capabilities

  • Protocol understanding
  • Information extraction
  • Drafting new sections
  • Identifying inconsistencies

Example prompts

  • "Summarize the inclusion/exclusion criteria from this clinical trial protocol." (followed by providing the protocol text)
  • "Generate a section on adverse event reporting for a Phase 3 oncology trial."
  • “Compare the primary endpoints of these two protocols and highlight any differences.”

Tips & gotchas

The skill's effectiveness depends heavily on the clarity and completeness of the input clinical trial protocol. Providing well-structured and formatted documents will yield better results.

Tags

🛡️

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Details

Version
vlatest
License
Author
anthropics
Installs
5

🏢 Official

Published by the company or team that built the technology.