NIH's TrialGPT cuts clinical trial patient screening time by 40% using large language models

National Institutes of Health (NIH) / National Library of Medicine deployed Large Language Models & Generative AI for Clinical Trials & Research in Pharmaceutical & Life Science. As reported by www.nih.gov: 40% patient screening time reduction.

Maintained by Peter Korpak, Lead EditorHow evidence is checked
40%Patient Screening Time Reduction
Equivalent (benchmarked on 1,000+ patient-criterion pairs)Accuracy vs. Human Clinicians

Source-reported figures (cited source: www.nih.gov)

What National Institutes of Health (NIH) / National Library of Medicine was trying to fix

Finding the right clinical trial for interested patients is a time-consuming and resource-intensive process for clinicians, slowing down important medical research. Clinicians must manually navigate the vast and ever-changing catalog of trials listed on ClinicalTrials.gov, assessing eligibility criteria against individual patient profiles.

What National Institutes of Health (NIH) / National Library of Medicine deployed

NIH researchers from NLM and the National Cancer Institute developed TrialGPT, an LLM-powered framework that processes a patient summary, identifies relevant trials from ClinicalTrials.gov, excludes ineligible ones, and generates an annotated ranked list of trials with eligibility explanations for clinician review.

Results

In a pilot user study, clinicians using TrialGPT spent 40% less time screening patients while maintaining the same level of accuracy as manual review. TrialGPT's criterion-level eligibility predictions achieved nearly the same accuracy as human clinicians when benchmarked against over 1,000 patient-criterion pairs.

Key Takeaways

  • LLMs can match clinician-level accuracy on structured eligibility screening tasks, enabling meaningful time savings without sacrificing precision.
  • Ranking and annotating trial matches — rather than just flagging eligibility — is key to making AI-assisted trial matching actionable for clinicians.
  • Responsible AI deployment in clinical research requires fairness evaluation across diverse and underrepresented populations before broad rollout.

Evidence for National Institutes of Health (NIH) / National Library of Medicine's Clinical Trials & Research deployment

Reported outcome metrics
2 cited below
Cited source
www.nih.gov
Last updated
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