Angiographic and Psychosocial Evaluation of Peripartum vs. Non: SCAD

Completed

Conditions studied: Spontaneous Coronary Artery Dissection

In brief

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.

Key facts

Study ID

NCT03390998

Run by

Katharine Sears Edwards

People needed

241

Starts

2017-11-28

Expected to finish

2019-05-31

Last updated by the study team

2019-09-25

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• Not fulfilling inclusion criteria

Where it is running

• Stanford University Medical Center — Palo Alto, California, United States

Full record on ClinicalTrials.gov

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