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Recruiting NCT06300450

NCT06300450 Randomized Controlled Trial of Alert-Based Computerized Decision Support for Patients With Peripheral Artery Disease Not Prescribed Lipid-Lowering Therapy

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Clinical Trial Summary
NCT ID NCT06300450
Status Recruiting
Phase
Sponsor Brigham and Women's Hospital
Condition Peripheral Artery Disease
Study Type INTERVENTIONAL
Enrollment 400 participants
Start Date 2023-03-01
Primary Completion 2026-12-28

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Computer Alert

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 400 participants in total. It began in 2023-03-01 with a primary completion date of 2026-12-28.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This single-center, 400-patient, randomized controlled trial assesses the impact of a patient- and provider-facing EPIC Best Practice Advisory (BPA; alert-based computerized decision support tool) to increase guideline-directed utilization of statin and statin-alternative oral LDL-C lowering therapies in patients with PAD who are not being prescribed LDL-C-lowering therapy.

Eligibility Criteria

Inclusion Criteria: * All patients ≥ 18 years old * Seen in Cardiovascular Medicine Clinic, Primary Care, Podiatry, Vascular Surgery, and Diabetology * Medical history entry, visit diagnosis, or problem list entry of PAD * Not prescribed LDL-C-lowering therapy Exclusion Criteria: * Patients taking a statin, ezetimibe, bempedoic acid, a PCSK9 inhibitor, inclisiran or a combination will be excluded

Contact & Investigator

Central Contact

Gregory Piazza

✉ gpiazza@bwh.harvard.edu

📞 6177326984

Principal Investigator

Gregory Piazza

PRINCIPAL INVESTIGATOR

BWH

Frequently Asked Questions

Who can join the NCT06300450 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Peripheral Artery Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06300450 currently recruiting?

Yes, NCT06300450 is actively recruiting participants. Contact the research team at gpiazza@bwh.harvard.edu for enrollment information.

Where is the NCT06300450 trial being conducted?

This trial is being conducted at Boston, United States.

Who is sponsoring the NCT06300450 clinical trial?

NCT06300450 is sponsored by Brigham and Women's Hospital. The principal investigator is Gregory Piazza at BWH. The trial plans to enroll 400 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology