Registry for spontaneous coronary artery dissection in Switzerland
Official title: Spontaneous Coronary Artery Dissection (SCAD) National Swiss Registry (SwissSCAD)
Run by University Hospital, Geneva · NCT04457544 · Data updated 2026-11-12
This study is creating a registry to collect information about spontaneous coronary artery dissection in Switzerland to help improve diagnosis and treatment for young women affected by this condition.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | University Hospital, Geneva Academic / other |
| Locations | 1 site (Geneva) |
| Status | Recruiting |
| Started | August 12, 2020 |
| Main results expected | June 30, 2025 |
| Study ends | June 30, 2030 |
| Registry record updated | November 16, 2022 |
| Trial ID | NCT04457544 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals aged 18 and older who have been newly diagnosed with SCAD or diagnosed within the last five years.
✕Probably not a fit
Patients with atherosclerotic or iatrogenic coronary dissection 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
This observational study aims to create a national registry for spontaneous coronary artery dissection (SCAD) in Switzerland. It focuses on understanding the natural history, outcomes, and treatments of SCAD, which primarily affects young women without traditional cardiovascular risk factors. By collecting data from patients diagnosed with SCAD, the registry seeks to improve timely diagnosis and clinical follow-up, addressing the gaps in knowledge surrounding this underdiagnosed condition. The study will include patients who are newly diagnosed or diagnosed within the last five years.
Why it matters
Potential benefit: If successful, this registry could lead to improved diagnosis and management of SCAD, ultimately reducing adverse cardiac outcomes.
How similar studies have gone: While SCAD is a relatively underexplored area, the establishment of registries has shown promise in other conditions, suggesting potential for success in this novel approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Subject is ≥18 years of age. * Patient presenting newly diagnosed SCAD or diagnosed with SCAD within the last 5 years. * Subject must be willing to sign a Patient Informed Consent (PIC). Exclusion Criteria: * Patient unwilling or unable to provide informed consent. * Patients with atherosclerotic or iatrogenic coronary dissection.
Where it's running
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Geneva University Hospitals
Geneva, Switzerland Recruiting
Study contacts
- Principal investigator: Sophie Degrauwe, Dr — Hopitaux universitaires de Geneve
- Study coordinator: Sophie Degrauwe, Dr
- Email: sophie.degrauwe@hcuge.ch
- Phone: +41795530294
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Survey of physical activity and quality of life for people with fibromuscular dysplasia
This national survey asks adults with fibromuscular dysplasia to see if activity restrictions affect their quality of life and emotional well-being.
-
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.
-
Stress contrast echocardiography in adults with prior SCAD
This project will use stress contrast echocardiography to see if small-vessel heart blood flow and blood-pressure responses during stress are different in adults who had spontaneous coronary artery dissection (SCAD) compared with healthy adults.
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Remote exercise program after spontaneous coronary artery dissection
This study tests a remote exercise program to see if it’s doable for women recovering from SCAD events.
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Registry for Spontaneous Coronary Artery Dissection
This study is setting up a large registry to collect information from women who have experienced spontaneous coronary artery dissection to better understand the condition and improve treatment options.
-
Analyzing the role of the sympathetic nervous system in spontaneous coronary artery dissection
This study is testing how the sympathetic nervous system affects heart health in people who have had spontaneous coronary artery dissection compared to similar individuals without the condition.
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.