SCADRegistry for Spontaneous Coronary Artery Dissection (SCAD) Patients
Data Collection
Arterial Occlusive Diseases+11
+ Arteriosclerosis
+ Cardiovascular Diseases
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: July 1, 2011
Actual date on which the first participant was enrolled.Spontaneous Coronary Artery Dissection (SCAD) is a condition that isn't well understood and tends to affect more women than men. It happens when two layers of the coronary arteries separate, allowing blood to flow into the space between them. This can block normal blood flow in the heart, leading to chest pain, heart attacks, and in some cases, sudden death. To better understand and prevent this potentially life-threatening event, Mayo Clinic is conducting studies on SCAD. One of these studies aims to build a database of patients with SCAD, regardless of whether they've been treated at Mayo Clinic or not. The goal is to identify patterns in SCAD occurrence, causes, and associations, which could guide future research and improve care for this condition. With the participant's consent, Mayo Clinic staff will request a copy of the original coronary angiogram, the test used to diagnose SCAD, to confirm the diagnosis and determine eligibility. If eligible, study coordinators will reach out to the participant to provide more information about the studies and request a signed informed consent document. The primary goal of this observational study is to gather data about SCAD-related risk factors, symptoms at diagnosis, treatments used, and long-term outcomes for patients.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.2500 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location