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Multidisciplinary Approach to Reduce Cardiovascular Health Disparities

Multidisciplinary Approach to Reduce Cardiovascular Health Disparities in the Baltimore RAcial Minority CommunitiEs (M-BRACE Trial)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06168968
Acronym
M-BRACE
Enrollment
400
Registered
2023-12-13
Start date
2023-02-06
Completion date
2025-12-31
Last updated
2024-11-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome, Ischemic Stroke, Multi Vessel Coronary Artery Disease

Brief summary

The goal of this observational study is to investigate the potential differences in thrombogenicity between black and white patients admitted with atherothrombotic events including acute coronary syndrome, multi-vessel coronary disease, and ischemic stroke. Participants will engage in laboratory testing and health outcome assessments.

Interventions

BEHAVIORALLife and Medication Recommendations

Based on obtained subjective and objective data from patient-filled questionnaire and laboratory testing respectively, lifestyle and medication recommendations will be provided for secondary prevention of cardiovascular and cerebrovascular diseases

Sponsors

University of Maryland
CollaboratorOTHER
LifeBridge Health
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients ≥18 years of age admitted with ACS, AIS, or multi-vessel CAD * Competent mental condition to provide informed consent and able to participate in follow-ups

Exclusion criteria

* Pregnant women * Currently enrolled in an investigational drug or device trial * Undergoing treatment for neoplastic, autoimmune, or connective tissue disease * COVID-19 infection within 30 days of enrollment * Known history of hepatitis or HIV * Deemed unfit to participate according to the investigator * Known history of drug abuse * Known platelet count of \<100,000/mm3 * Hematocrit \< 25%

Design outcomes

Primary

MeasureTime frameDescription
Differences in Platelet Fibrin Clot Formation (MA,mm)BaselineDifferences in Platelet Fibrin Clot Formation (MA,mm) Between Black and White Patients
Differences in Speed of Clot Formation (R, min)BaselineDifferences in Speed of Clot Formation (R, min) Between Black and White Patients

Secondary

MeasureTime frameDescription
Major Adverse Cardiovascular Events Post Index Hospitalization3 and 12 months post index hospitalizationMajor Adverse Cardiovascular Events (death, MI, stroke, unplanned target vessel revascularization, major bleeding) Post Index Hospitalization

Countries

United States

Contacts

Primary ContactKevin Bliden, BS, MBA
kbliden@lifebridgehealth.org4432441497

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026