Mayo Clinic
Rochester, Minnesota, 55905, United States
Location status: Recruiting
Location contact
Marysia S Tweet, M.D., M.S.
PRINCIPAL_INVESTIGATOR
Susan Milbrandt
CONTACT
NCT Number: NCT01429727
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.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Rochester, Minnesota, 55905, United States
Location status: Recruiting
Marysia S Tweet, M.D., M.S.
PRINCIPAL_INVESTIGATOR
Susan Milbrandt
CONTACT
Spontaneous Coronary Artery Dissection (SCAD) is a relatively rare and poorly understood condition that has been reported to affect more women than men. The coronary arteries consist of three layers, and dissection occurs when two of these layers separate, enabling blood to flow into the space between the layers. As the blood accumulates, this can cause obstruction to normal blood flow within the heart, leading to chest pain, heart attack and even sudden death.
The medical community has much to learn about treatment and prevention of this potentially fatal cardiovascular event. Mayo Clinic is conducting two studies of SCAD. This study consists of building a database/registry of patients with SCAD (whether they have been patients at Mayo Clinic or not) to identify patterns of SCAD incidence, causes and associations that could guide future research. With participant consent, Mayo Clinic staff will request a copy of the original coronary angiogram when SCAD was diagnosed to confirm the diagnosis and determine eligibility. If eligible, study coordinators will contact the participant to provide more information about the studies and request a signed informed consent document.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Persons with history of SCAD who are interested in participating in the study but do not meet the updated inclusion criteria will not be enrolled at this time. However, they will be given the option to share their contact information in order to be invited to future Mayo Clinic SCAD studies.
Time frame: Continuous time frame following index event for 2-10 years from study contact date.
Obtain data regarding SCAD related risk factors, presenting characteristics, treatments and long term outcomes.
Time frame: Continuous time frame following index event for 2-10 years from study contact date.
Record update on patient's current physical health and any relevant health events that may have occurred since the initial SCAD event.
Time frame: Continuous time frame following index event for 2-10 years from study contact date.
Record update on patient's current mental health status since the initial SCAD event.
Contact information is provided by the study sponsor or research team.
Mayo Clinic
Other
Acronym: SCAD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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