RECRUITINGOBSERVATIONAL
International Spontaneous Coronary Artery Dissection (SCAD) "iSCAD" Registry
The International Spontaneous Coronary Artery Dissection "iSCAD" Registry (SCAD)
About This Trial
The aim of "iSCAD," the International Spontaneous Coronary Artery Dissection (SCAD) Registry, is to serve as an internationally collaborative, multicenter registry coordinated by an experienced and centralized coordinating center in an effort to increase the pace of participant recruitment, and thereby increase statistical power of studies related to SCAD. The ultimate goal of iSCAD Registry is to facilitate the development of best practices and clinical guidelines for preventing SCAD or its recurrence. This observational study will be prospective and retrospective in its recruitment and will collect clinical information to better understand the natural history and prognosis for SCAD.
Who May Be Eligible (Plain English)
Who May Qualify:
Participants with a new diagnosis of SCAD or a history of confirmed or suspected SCAD will be prospectively recruited from either:
1. Inpatient wards of the enrolling medical centers during the acute presentation of SCAD, or
2. Outpatient cardiovascular clinics of enrolling medical centers.
Participants must be:
- 18 years of age or older
- Diagnosis of SCAD or history of SCAD based on coronary angiography, either catheter-based or coronary CTA
- Suspected SCAD by coronary angiography
Who Should NOT Join This Trial:
1. Coronary dissection in association with atherosclerosis or as a result of iatrogenic injury
2. Inability to provide willing to sign a consent form
3. Inability to complete study-related patient questionnaires
4. Inability to understand and complete patient questionnaires independently
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
Participants with a new diagnosis of SCAD or a history of confirmed or suspected SCAD will be prospectively recruited from either:
1. Inpatient wards of the enrolling medical centers during the acute presentation of SCAD, or
2. Outpatient cardiovascular clinics of enrolling medical centers.
Participants must be:
* 18 years of age or older
* Diagnosis of SCAD or history of SCAD based on coronary angiography, either catheter-based or coronary CTA
* Suspected SCAD by coronary angiography
Exclusion Criteria:
1. Coronary dissection in association with atherosclerosis or as a result of iatrogenic injury
2. Inability to provide informed consent
3. Inability to complete study-related patient questionnaires
4. Inability to understand and complete patient questionnaires independently
Locations (20)
Cedars Sinai
Los Angeles, California, United States
UCLA (University of California, Los Angeles)
Los Angeles, California, United States
Kaiser Permanente Northern California
San Francisco, California, United States
University of Colorado
Aurora, Colorado, United States
Hartford Hospital
Hartford, Connecticut, United States
University of South Florida
Tampa, Florida, United States
Emory Healthcare System
Atlanta, Georgia, United States
Northwestern Medicine
Chicago, Illinois, United States
University of Kentucky
Lexington, Kentucky, United States
Johns Hopkins
Baltimore, Maryland, United States
Massachusetts General Hospital
Boston, Massachusetts, United States
St. Luke's Mid America
Kansas City, Missouri, United States
Washington University
St Louis, Missouri, United States
Dartmouth-Hitchcock
Lebanon, New Hampshire, United States
Catholic Medical Center
Manchester, New Hampshire, United States
Mount Sinai
New York, New York, United States
Columbia University Medical Center
New York, New York, United States
Atrium Health Sanger Heart and Vascular Institute
Charlotte, North Carolina, United States
University Hospitals--Case Western
Cleveland, Ohio, United States
Oklahoma Heart
Oklahoma City, Oklahoma, United States