Clinical trial Recruiting at 1 site Interventional

AI-driven clinical decision support to reduce hospital-acquired blood clots

Official title: AI-driven Clinical Decision Support to Reduce Hospital-Acquired Venous Thromboembolism

Run by Vanderbilt University Medical Center · NCT06939803 · Data updated 2026-11-12

This project will test whether an automated AI tool that flags hospitalized adults at risk can help clinicians prevent hospital-acquired blood clots at Vanderbilt hospitals.

Quick facts

Study typeInterventional
SexAll
Enrollment2236 (estimated)
SponsorVanderbilt University Medical Center
Academic / other
Locations1 site (Nashville, Tennessee)
StatusRecruiting
StartedDecember 17, 2025
Main results expectedDecember 16, 2026
Study endsMarch 31, 2027
Registry record updatedFebruary 13, 2026
Trial IDNCT06939803 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adult inpatients at the listed Vanderbilt hospitals who are not currently receiving thromboprophylaxis and have no contraindication to prophylaxis.

Probably not a fit

Patients already on appropriate blood-clot prevention, those with contraindications to prophylaxis, or patients admitted outside the Vanderbilt system are unlikely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The VTE-AI randomized trial embeds an automated risk model into the electronic health record and randomizes inpatients to receive AI-driven clinical decision support alerts versus usual care. The VTE-AI algorithm computes admission and daily risk scores without clinician input and prompts clinicians to reconsider thromboprophylaxis when no orders exist and there are no contraindications. The primary outcome is the incidence of hospital-acquired venous thromboembolism during the hospital stay across Vanderbilt's urban and rural hospitals. The trial enrolls adult inpatients admitted to Vanderbilt University Medical Center and participating affiliated hospitals with no prespecified exclusions.

Why it matters

Potential benefit: If successful, the tool could lower the number of hospital-acquired blood clots, reduce complications and deaths, and decrease related healthcare costs.

How similar studies have gone: Previous prognostic models for HA-VTE have shown mixed performance, and while the VTE-AI score was retrospectively validated by the Vanderbilt team, randomized evidence that AI-driven alerts reduce HA-VTE is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Inpatient admission to Vanderbilt Adult Hospital, Vanderbilt Tullahoma Harton Hospital, Vanderbilt Bedford County Hospital, or Vanderbilt Wilson County Hospital

Exclusion Criteria:

* None

Where it's running

  • Vanderbilt University Medical Center
    Nashville, Tennessee, United States
    Recruiting

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.