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Clinical Trial Literature Search

Professional Updated 2026.08.29

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Please install @user_ff7413f5/ct-literature according to https://skillhub.cn/install/skillhub.md.

About this skill

Problem It Solves

When preparing trial planning, protocol/CSR background, or published-safety checks, evidence is scattered across OpenAlex, Europe PMC, and preprints; fields are inconsistent, records duplicate, citations can be hard to verify, and published safety literature is easily mistaken for a FAERS signal. This skill turns published-evidence retrieval into a repeatable JSON/Excel/HTML workflow.

How It Works

  • Multi-source public literature search: uses OpenAlex as the primary source, keeps Europe PMC on by default, and can enable --cochrane, --with-biorxiv, --with-arxiv, and other opt-in sources.
  • Normalization and de-duplication: merges records by DOI or title while preserving provenance, PubMed/PMC ID, abstracts, OA full-text URLs, MeSH terms, keywords, funders, and other structured fields.
  • Evidence packaging: outputs lit_report.xlsx, lit_report.html, and references.bib / references.ris; --prisma can generate a PRISMA funnel, and --rank relevance scores title/abstract relevance.
  • Safety and citation verification: --safety is only a qualitative filter for published AE/PV literature, while --verify checks citations against DOI, Crossref, Europe PMC, and other sources to reduce hallucination.

Boundaries

  • Reads public bibliographic APIs only; it does not fetch registry structured metadata or perform FAERS disproportionality analysis.
  • Defaults to SAFE PREVIEW; network requests require explicit --run. OpenAlex keyless access is quota-limited, so a local .env key is recommended.
  • Guideline content is a local pointer-only corpus rather than a live latest-guideline fetch; PROSPERO/NICE/TRIP may be skipped due to token or documentation limits.
  • Output is for background reference only and is not a regulatory submission.

Use Cases

  • Before drafting an indication protocol, retrieve published systematic reviews and RCTs, then export a de-duplicated master list.
  • Prepare a CSR safety section by filtering published AE/PV literature into a qualitative subset using --safety.
  • Verify paper citations by checking DOI, title, and author consistency with --verify.
  • Search Cochrane reviews using --cochrane and generate a PRISMA screening funnel in the HTML report.

Best For

  • Clinical medical writers who need published background evidence for protocols or CSRs.
  • Pharmacovigilance staff who need published AE/PV literature for qualitative reference.
  • Clinical researchers who need a quick evidence landscape for a disease, drug, or method.
  • Research data engineers who need multi-source de-duplication, structured exports, and citation verification.