RECRUITING

International Spontaneous Coronary Artery Dissection (SCAD) "iSCAD" Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

The International Spontaneous Coronary Artery Dissection "iSCAD" Registry (SCAD)

Quick Facts

Study Start:2019-03-08
Study Completion:2025-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04496687

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Inpatient wards of the enrolling medical centers during the acute presentation of SCAD, or
  2. 2. Outpatient cardiovascular clinics of enrolling medical centers.
  3. * 18 years of age or older
  4. * Diagnosis of SCAD or history of SCAD based on coronary angiography, either catheter-based or coronary CTA
  5. * Suspected SCAD by coronary angiography
  1. 1. Coronary dissection in association with atherosclerosis or as a result of iatrogenic injury
  2. 2. Inability to provide informed consent
  3. 3. Inability to complete study-related patient questionnaires
  4. 4. Inability to understand and complete patient questionnaires independently

Contacts and Locations

Study Contact

Esther Kim, MD, MPH
CONTACT
704-373-0212
Soo.Kim@atriumhealth.org

Principal Investigator

Esther Kim, MD
STUDY_CHAIR
Chair, Steering Committee
Malissa Wood, MD
PRINCIPAL_INVESTIGATOR
Member, Steering Committee
Sahar Naderi, MD
PRINCIPAL_INVESTIGATOR
Member, Steering Committee

Study Locations (Sites)

Cedars Sinai
Los Angeles, California, 90048
United States
UCLA (University of California, Los Angeles)
Los Angeles, California, 93003
United States
Kaiser Permanente Northern California
San Francisco, California, 94115
United States
University of Colorado
Aurora, Colorado, 80045
United States
Hartford Hospital
Hartford, Connecticut, 06106
United States
University of South Florida
Tampa, Florida, 33602
United States
Emory Healthcare System
Atlanta, Georgia, 30308
United States
Northwestern Medicine
Chicago, Illinois, 60611
United States
University of Kentucky
Lexington, Kentucky, 40508
United States
Johns Hopkins
Baltimore, Maryland, 21224
United States
Massachusetts General Hospital
Boston, Massachusetts, 02114-2696
United States
St. Luke's Mid America
Kansas City, Missouri, 64111
United States
Washington University
Saint Louis, Missouri, 63110
United States
Dartmouth-Hitchcock
Lebanon, New Hampshire, 03756
United States
Catholic Medical Center
Manchester, New Hampshire, 03102
United States
Mount Sinai
New York, New York, 10029-6574
United States
Columbia University Medical Center
New York, New York, 10032
United States
Atrium Health Sanger Heart and Vascular Institute
Charlotte, North Carolina, 28204
United States
University Hospitals--Case Western
Cleveland, Ohio, 44106
United States
Oklahoma Heart
Oklahoma City, Oklahoma, 73120
United States
Providence
Portland, Oregon, 97225
United States
University of Pennsylvania
Philadelphia, Pennsylvania, 19104
United States
Allegheny General Hospital, Allegheny Health Network
Pittsburgh, Pennsylvania, 15212
United States
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, 15213
United States
Vanderbilt University Medical Center
Nashville, Tennessee, 37232
United States
UT Southwestern
Dallas, Texas, 75390
United States
Intermountain
Murray, Utah, 84107
United States
University of Virginia
Charlottesville, Virginia, 22908
United States
Inova Heart & Vascular Institute
Fairfax, Virginia, 22031
United States
University of Washington Medicine
Seattle, Washington, 98195
United States

Collaborators and Investigators

Sponsor: SCAD Alliance

  • Esther Kim, MD, STUDY_CHAIR, Chair, Steering Committee
  • Malissa Wood, MD, PRINCIPAL_INVESTIGATOR, Member, Steering Committee
  • Sahar Naderi, MD, PRINCIPAL_INVESTIGATOR, Member, Steering Committee

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-03-08
Study Completion Date2025-12-31

Study Record Updates

Study Start Date2019-03-08
Study Completion Date2025-12-31

Terms related to this study

Keywords Provided by Researchers

  • spontaneous coronary artery dissection (SCAD)
  • myocardial infarction
  • sudden cardiac arrest
  • acute coronary syndrome

Additional Relevant MeSH Terms

  • Spontaneous Coronary Artery Dissection