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NCT Number: NCT06300450

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Brigham and Women's Hospital

Boston, Massachusetts, 02115, United States

Location status: Recruiting

Location contact

Gregory Piazza, MD, MS

CONTACT

[email protected]

617-732-6984

Gregory Piazza, MD, MS

PRINCIPAL_INVESTIGATOR

Jorge Plutzky, MD

SUB_INVESTIGATOR

Ron Blankstein, MD

SUB_INVESTIGATOR

Samuel Goldhaber, MD

SUB_INVESTIGATOR

CONTACT

[email protected]

About this study

A Joint Task Force from the European Atherosclerosis Society and the European Society of Vascular Medicine recommends a low-density lipoprotein cholesterol (LDL-C) goal reduction of greater than 50% from baseline and a target of 55 mg/dL in patients with peripheral artery disease (PAD). An analysis of 1982 provider visits of patients with PAD in national outpatient databases in the U.S. between 2005-2012 showed that a statin was prescribed in only 33.1% of patients (Berger JS, Ladapo JA. J Am Coll Cardiol. 2017;69:2293-2300). Data from Europe demonstrates marginally better adherence to guidelines with 40% of patients with PAD prescribed a statin (Subherwal S, et al. Circulation. 2012;126:1345).

Explanations for underutilization of LDL-C-lowering therapy in patients with PAD include clinician knowledge gaps regarding evidence-based clinical practice guideline recommendations, provider inertia, the need for prior authorization for some agents, statin intolerance, and statin hesitancy. Statin intolerance is defined as the inability to tolerate a dose of statin required to sufficiently reduce cardiovascular risk and has been estimated to affect up to 15% of patients treated with statins (Banach M, et al. Arch Med Sci 2015;11:1-23 and Banach M, et al. Expert Opin Drug Saf 2015;14:935-55). While numerous statin options exist and non-statin oral options for LDL-C lowering, such as ezetimibe and bempedoic acid, are widely available, lack of awareness and inconsistent implementation contribute to underutilization in patients at high-risk for cardiovascular events, such as those with PAD. Bempedoic acid, with or without ezetimibe, is a newer option for LDL-C lowering that offers a lower prevalence of musculoskeletal side effects than statins (Diabetes Ther. 2021 Jul;12(7):1779-1789). However, familiarity with this option remains limited outside of Preventive Cardiology and Lipid Clinics.

The failure to achieve guideline-directed LDL-C targets due to clinician knowledge gaps, provider inertia, the need for prior authorization, statin intolerance, and statin hesitancy in the PAD population demonstrates similar clinical obstacles to other areas of cardiovascular medicine in which quality of care was impacted by provider and patient knowledge gaps. An alert-based computerized decision support (CDS) approach has been shown to be effective in such circumstances and could be similarly effective for optimizing lipid management in patients with PAD.

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Computer Alert

Behavioral

On-screen alert-based decision support raising awareness of need for lipid-lowering therapy in patients with peripheral artery disease

Other names: EPIC Best Practice Advisory

Primary outcomes

  1. Frequency of prescription of oral LDL-C-lowering therapy

    Time frame: 90 days

    The frequency of prescription of oral LDL-C-lowering therapy will be assessed using a report from the medical record

Secondary outcomes

  1. Change in LDL-C level

    Time frame: 6 months

    Change in LDL-C level will be assessed via the medical record

Other outcomes

  1. Frequency of all-cause mortality

    Time frame: 6 months

    The frequency will be assessed using a report from the medical record

  2. Frequency of major adverse cardiovascular events

    Time frame: 6 months

    The frequency of major adverse cardiovascular events (including myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization) will be assessed using a report from the medical record

  3. Frequency of major adverse limb events

    Time frame: 6 months

    The frequency of major adverse limb events (including amputation and peripheral artery revascularization) will be assessed using a report from the medical record

  4. Frequency of all-cause hospitalization

    Time frame: 6 months

    The frequency of all-cause hospitalization will be assessed using a report from the medical record

Study contacts

Contact information is provided by the study sponsor or research team.

Candrika D Kharaini

CONTACT

cdkhairani@@bwh.harvard.edu

6177326984

Gregory Piazza

CONTACT

[email protected]

6177326984

Sponsors and collaborators

Lead sponsor

Brigham and Women's Hospital

Other

Collaborators

  • Esperion Therapeutics, Inc.

Registry information

Acronym: PAD-ALERT

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Mar 8, 2024
Registry last updated
Jun 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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