Advancing Cardiac Care Unit-based Rapid Assessment and Treatment of hypErcholesterolemia
NCT05218005 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 140
Last updated 2026-05-01
Summary
ACCURATE will test the hypothesis that opportunistic genetic testing for Familial Hypercholesterolemia (FH) in patients admitted to hospital with an acute coronary syndrome will increase the diagnosis of FH and will impact patient care and outcomes. The study will recruit patients admitted to hospital with an acute coronary syndrome, and research-based genetic testing will be conducted for known FH-causing genetic variants. The results will be returned to the patients' treating physicians. The primary endpoint will be the number of patients with a new diagnosis of definite FH. The secondary endpoints will be the proportion of patients who undergo intensification of lipid-lowering therapy, the lowest LDL cholesterol level achieved, and the proportion of patients reaching guideline recommended lipid targets in the 15 months after the index acute coronary syndrome.
Conditions
- Familial Hypercholesterolemia
- Familial Hypercholesterolemia Due to Genetic Defect of Apolipoprotein B
- Familial Hypercholesterolemia Due to Heterozygous LDL Receptor Mutation
- Familial Hypercholesterolemia - Heterozygous
- Acute Coronary Syndrome
- NSTEMI - Non-ST Segment Elevation MI
- STEMI
- Familial Hypercholesterolemia With Hyperlipemia
Interventions
- DIAGNOSTIC_TEST
-
Research-based genetic test for Familial Hypercholesterolemia
Next-generation targeted sequencing assay to identify DNA variants in genes known to cause Familial Hypercholesterolemia
Sponsors & Collaborators
-
Genome British Columbia
collaborator INDUSTRY -
Vancouver Coastal Health Research Institute
collaborator OTHER -
University of British Columbia
lead OTHER
Principal Investigators
-
Liam Brunham, MD PhD · University of British Columbia
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-01-01
- Primary Completion
- 2024-06-17
- Completion
- 2025-08-29
Countries
- Canada
Study Locations
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