RECRUITING

The "Virtual" Multicenter Spontaneous Coronary Artery Dissection (SCAD) Registry

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Conditions

Spontaneous Coronary Artery DissectionSCADcoronary artery diseasemyocardial infarctioncoronary dissection

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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 primary goal of this project is to describe the clinical and physiologic characteristics of Spontaneous Coronary Artery Dissections (SCAD) in order to increase awareness, understanding, treatment and prevention of a potentially fatal cardiovascular event. This study will be a retrospective and prospective review of medical course and current health of men and women with SCAD.

Official Title

The "Virtual" Multicenter Spontaneous Coronary Artery Dissection (SCAD) Registry

Quick Facts

Study Start:2011-07
Study Completion:2030-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT01429727

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Men and women able to give informed consent
  2. * Diagnosis of one or more episodes of spontaneous coronary artery dissection (SCAD)
  3. * SCAD in women who are pregnant or within 12 months postpartum at the time of SCAD
  4. * SCAD in individuals who self-identify as a member of a racial or ethnic group that is currently underrepresented in the registry. This would include anyone who identifies as: Black/African American, Asian, American Indian, or Alaska Native, Native Hawaiian, or Other Pacific Islander, and any race with Hispanic ethnicity
  5. * SCAD in a man
  6. * SCAD in persons younger than 30 years of age
  7. * SCAD within the past 2 weeks (acute)
  8. * SCAD patient enrolling into any other Mayo Clinic SCAD Research Study
  9. * SCAD in individuals who have a relative that has had a SCAD event
  1. * Lack of angiographic confirmation of SCAD
  2. * Iatrogenic dissection or an alternate diagnosis

Contacts and Locations

Study Contact

Susan Milbrandt
CONTACT
507-266-3180
mayoscad@mayo.edu

Principal Investigator

Sharonne N. Hayes, M.D.
PRINCIPAL_INVESTIGATOR
Mayo Clinic

Study Locations (Sites)

Mayo Clinic
Rochester, Minnesota, 55905
United States

Collaborators and Investigators

Sponsor: Mayo Clinic

  • Sharonne N. Hayes, M.D., PRINCIPAL_INVESTIGATOR, Mayo Clinic

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 Date2011-07
Study Completion Date2030-12

Study Record Updates

Study Start Date2011-07
Study Completion Date2030-12

Terms related to this study

Keywords Provided by Researchers

  • Spontaneous coronary artery dissection
  • SCAD
  • coronary artery disease
  • myocardial infarction
  • coronary dissection

Additional Relevant MeSH Terms

  • Spontaneous Coronary Artery Dissection
  • SCAD