Observational study on spontaneous coronary artery dissection
Official title: Canadian Spontaneous Coronary Artery Dissection (SCAD) Study and Genetic Sub-study (Prospective, Observational Registry With 10 Year Follow-up)
Run by Cardiology Research UBC · NCT04906356 · Data updated 2026-11-12
This study is trying to learn more about spontaneous coronary artery dissection (SCAD) by following 3,000 patients over 10 years to better understand who it affects and how to treat it.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 3000 (estimated) |
| Sponsor | Cardiology Research UBC Academic / other |
| Locations | 1 site (Vancouver, British Columbia) |
| Status | Recruiting |
| Started | December 1, 2018 |
| Main results expected | December 1, 2033 |
| Study ends | December 1, 2033 |
| Registry record updated | May 28, 2021 |
| Trial ID | NCT04906356 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients admitted with acute coronary syndrome who have documented SCAD on a coronary angiogram.
✕Probably not a fit
Patients whose SCAD is attributed to atherosclerotic coronary artery disease will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The Canadian SCAD Study is a multicenter, prospective observational registry aimed at understanding the natural history of spontaneous coronary artery dissection (SCAD) and its associated conditions. This study will enroll 3,000 patients over a 10-year follow-up period, focusing on the demographics, predisposing factors, and treatment strategies for SCAD. By collecting data from major cardiac centers across Canada and internationally, the study seeks to address the gaps in knowledge regarding SCAD, which often affects young women and is frequently misdiagnosed. The findings will help inform future randomized controlled trials and improve management strategies for SCAD patients.
Why it matters
Potential benefit: If successful, this study could lead to better diagnosis and management strategies for patients suffering from SCAD.
How similar studies have gone: While SCAD has been under-researched, this study builds on previous efforts and aims to fill significant knowledge gaps, making it a novel approach in this area.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients admitted with ACS (STEMI, NSTEMI or unstable angina) 2. Documented SCAD on a coronary angiogram (including diagnosis with OCT or IVUS) Exclusion Criteria: 1\. Patients where SCAD is attributed to atherosclerotic coronary artery disease, with atherosclerotic coronary artery disease stenosis ≥50%
Where it's running
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Vancouver General Hospital
Vancouver, British Columbia, Canada Recruiting
Study contacts
- Principal investigator: Jacqueline Saw, MD — Cardiology Research UBC / Vancouver General Hospital
- Study coordinator: Andrew Starovoytov, MD
- Email: a.starovoytov@ubc.ca
- Phone: 6048755079
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Exercise responses in people with spontaneous coronary artery dissection or fibromuscular dysplasia
This study will test whether short sessions of different aerobic and resistance exercise change breathing, heart and blood pressure responses and symptoms in people with SCAD or FMD.
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Registry for Spontaneous Coronary Artery Dissection
This study is trying to gather information about people with Spontaneous Coronary Artery Dissection to better understand the condition and improve treatment and prevention.
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Genetic causes of spontaneous coronary artery dissection
This project will test whether inherited or new gene changes cause spontaneous coronary artery dissection in adults with SCAD and their biological relatives.
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Norwegian SCAD follow-up and outcomes program
This program will follow adults hospitalized with SCAD in Norway for one year to see if scheduled imaging, tests, and questionnaires identify complications and risk factors.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.