- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03876847
Genetics of Spontaneous Coronary Artery Dissection (SCAD-INSPIRE Genetics) (SCAD-INSPIRE)
Genetics of Spontaneous Coronary Artery Dissection (SCAD-INSPIRE Genetics): A Substudy of the INSPIRE Registry
Study Overview
Status
Conditions
Detailed Description
For this study, we will ascertain clinical data and biological samples from a cohort of SCAD patients identified using retrospective review of medical records and prospective surveillance of Intermountain patients that undergo coronary angiography. The SCAD diagnosis will be based on independent review of clinical presentation, cardiac imaging, and angiography findings by two cardiologists and a third cardiologist in case of disagreement. It is anticipated that we hope to recruit 100 SCAD patients.
Enrollment of these subjects will be done under the INSPIRE registry. The subjects will be asked to sign a consent, provide biological samples, and complete questionnaires related to SCAD as part of the INSPIRE registry.
The SCAD cases will be matched to records in the Intermountain Genealogy Registry (IGR) to allow for the identification of possible high-risk SCAD families. Risk of first and second degree relatives will also be assessed. The obtained blood samples will be processed, stored and genotyped.
Study Type
Enrollment (Estimated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
SCAD Cases
- Subjects of all ages, gender, or race
- Subjects had coronary angiography.
- Subjects had suspected SCAD as based on clinical report.
Controls
- INSPIRE subject that had coronary angiography at Intermountain Healthcare for stable angina.
- Subjects had no or mild atherosclerotic heart disease at time of angiography.
- Age at last visit as recorded in the Intermountain EDW at least 50 years or older.
- Not screened as possibly having a SCAD or coronary artery dissection diagnosis.
Exclusion Criteria:
SCAD Cases
- Independent review of cardiac imaging and clinical presentation by three cardiologists determine the coronary angiography was not a result of SCAD.
- Imaging from time of coronary angiography of poor quality as to not allow for proper determination of SCAD.
- Inability to determine criteria as outlined above.
- Subjects that have had a heart transplant.
- Subjects that have had a bone marrow transplant.
- Inability or refusal of the patient and/or the patient's legally acceptable representative to provide informed consent or blood sample for any reason.
- Other conditions that in the opinion of the Principal Investigator may increase risk to the subject and/or compromise the quality of the trial.
Controls
- Subjects that have a heart transplant.
- Subjects that have a bone marrow transplant.
Subjects with any of the following diagnosis at anytime
- Heart failure
- Heart valve disease
- Thoracic aortic aneurysm and dissection
- Ehlers-Danlos syndrome
- Shprintzen-Goldberg syndrome
- Marfan syndrome
- Loeys-Dietz aortic aneurysm syndrome
- Arterial tortuosity syndrome
Study Plan
How is the study designed?
Design Details
- Observational Models: Family-Based
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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Spontaneous Coronary Artery Disection
The spontaneous coronary artery disection (SCAD) diagnosis will be based on independent review of clinical presentation, cardiac imaging, and angiography findings by three cardiologists.
The determination will be evidence of linear luminal defect (intimal flap) detection, luminal narrowing or occlusion confirmed to be a dissection on further imaging, or by clinical judgment classifying it as definite SCAD.
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Control
A set of controls will be used for genetic analysis.
These controls will pulled from subjects in the INSPIRE registry that had coronary angiography at Intermountain Medical Center for stable angina and meet inclusion/exclusion criteria.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Genetic variants
Time Frame: at enrollment
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To determine genetic variants among spontaneous coronary artery dissection (SCAD) patients, we will do genotyping including target sequencing and whole exome/genome sequencing on samples provided by SCAD patients.
The primary focus of this sequencing will be to determine rates of variants in genes that cause cardiac-related connective tissue disorders.
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at enrollment
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1050343
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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