Trial Search Results

Angiographic and Psychosocial Evaluation of Peripartum vs. Non: SCAD

This multi-site international clinical research project is a collaboration between investigators from multiple institutions in the USA, Canada, and Europe. Approximately 7 to 11 sites will participate and provide data for analysis. Clinical operations (for data collection and analysis) across sites will be managed by Stanford. The study purpose is to determine differences in clinical and imaging presentation, in-hospital management and prognosis in peripartum and non-peripartum SCAD patients.

Stanford is currently accepting patients for this trial.

Lead Sponsor:

Katharine Sears Edwards

Collaborator: Vanderbilt University Medical Center

Stanford Investigator(s):

Eligibility


Inclusion Criteria:

Sites contacting patients and/or conducting the survey

   - Female adults 18 years of age and older

   - Voluntary participation

   - Patients with a known or suspected diagnosis of SCAD

   - Ability to read in English

   - Ability to access online consent and questionnaire portal

Sites not contacting patients and/or conducting the survey

   - Female adults 18 years of age and older

   - Patients with a known or suspected diagnosis of SCAD

Exclusion Criteria

- Not fulfilling inclusion criteria

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

Female

Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Recruiting