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NCT Number: NCT07334834

Implementation of an Algorithm- and Multi-professional Team-supported Strategy to Improve Lipid Management of Patients With Atherosclerotic Cardiovascular Disease

This is a randomized, controlled, collaborative, multicenter, pilot implementation science study evaluating the hypothesis that algorithm- and multi-professional team-supported lipid management reduces low density lipoprotein-cholesterol (LDL-C) compared with usual care in patients with atherosclerotic cardiovascular disease (ASCVD).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Colorado Health System (UCHealth)

Aurora, Colorado, 80045, United States

Location status: Recruiting

Location contact

Marc Bonaca, MD

CONTACT

About this study

OPTIMIZE-ASCVD is a randomized, controlled, collaborative, open-label, multicenter pilot implementation science study evaluating the hypothesis that algorithm- (Appendix A) and multi-professional team-supported lipid management reduces LDL-C compared with usual care in patients with ASCVD.

Approximately 100 participants will be randomized (1:1).

  • Participant preference for injectable vs oral lipid therapy will be recorded at baseline.
  • Participants allocated to algorithm-and multi-professional team-supported lipid management will be evaluated by a physician and prescribed lipid therapy which aims to achieve LDL-C target without titration. Participants will be contacted by a pharmacist to provide education about the medication and support any access issues.
  • Participants allocated to usual care will be referred for management by their usual care provider who will receive a summary of guideline recommendations

The study will include decentralized clinical trial features including use of local, Clinical Laboratory Improvement Amendments (CLIA)-certified laboratories for blood tests, use of data extracted from the electronic medical record (EMR), electronic collection of patient-reported outcomes (PRO) and remote conduct of study activities. As an open label study with both strategy groups receiving GDMT, no Data and Safety Monitoring Committee will be convened. Study leadership will monitor aggregate data during the trial and may modify the sample size and/or cap enrollment of subgroups to ensure consistency with design assumptions.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Provided informed consent
  • Age >18 years inclusive at screening
  • Documented atherosclerotic vascular disease including:
  • Coronary artery disease (prior revascularization, myocardial infarction, imaging evidence of coronary atherosclerosis)
  • Peripheral artery disease (prior revascularization, amputation, ankle: brachial index (ABI) ≤ 0.90, imaging evidence of extra-coronary atherosclerosis)
  • Carotid artery disease (prior endarterectomy or stenting of the extracranial carotid artery or imaging evidence of carotid atherosclerosis)
  • Imaging evidence of atherosclerotic vascular disease in a non-coronary vascular bed (e.g. aorta, mesenteric, renal)
  • LDL-C >70mg/dL

Exclusion criteria

  • Any reason that, in the opinion of the investigator, the patient would be unable to adhere to the protocol for the duration of the study (e.g. terminal diagnosis, metastatic cancer) or in whom participation might result in harm.
  • Planned active titration of current lipid-lowering therapy
  • Myocardial infarction or arterial revascularization within prior 30 days

Treatment and study plan

Algorithm- and multi-professional team-supported lipid management

Other

Algorithm- and multi-professional team-supported lipid management

Other names: Experimental

Guideline-directed lipid management by usual care provider

Other

Guideline-directed lipid management by usual care provider

Other names: Control

Primary outcomes

  1. The between group difference in LDL-C percent change

    Time frame: Baseline to 3 months

Secondary outcomes

  1. Between group difference

    Time frame: Baseline to 1 and 6 months

    LDL-C percent change

  2. Between group difference

    Time frame: 1, 3 and 6 months

    The proportion achieving LDL-C <55 mg/dL

  3. Between group difference

    Time frame: 1, 3 and 6 months

    Proportion receiving combination lipid lowering Therapy

Study contacts

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

Marc Bonaca, MD

CONTACT

[email protected]

(303) 860-9900

Sivan Naveh, MD. RPV

CONTACT

[email protected]

720-848-5300

Sponsors and collaborators

Lead sponsor

Colorado Prevention Center

Other

Registry information

Official study title

Implementation of an Algorithm- and Multi-professional Team-supported Strategy to Improve Lipid Management of Patients With Atherosclerotic Cardiovascular Disease: OPTIMIZE ASCVD

Acronym: OPTIMIZE ASCVD

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jan 12, 2026
Registry last updated
Jan 23, 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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