Education and Training
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.
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