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Angiographic and Psychosocial Evaluation of Peripartum vs. Non: SCAD

NCT03390998 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 241

Last updated 2019-09-25

No results posted yet for this study

Summary

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.

Conditions

  • Spontaneous Coronary Artery Dissection

Sponsors & Collaborators

  • Massachusetts General Hospital

    collaborator OTHER

  • Mayo Clinic

    collaborator OTHER

  • University Hospital, Clermont-Ferrand

    collaborator OTHER

  • University of British Columbia

    collaborator OTHER

  • University of Leicester

    collaborator OTHER

  • Vanderbilt University Medical Center

    collaborator OTHER

  • Katharine Sears Edwards

    lead OTHER

Principal Investigators

  • Jennifer Ann Tremmel, MD, MS · Stanford University

  • Katharine S. Edwards, PhD · Stanford University

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-28
Primary Completion
2019-05-31
Completion
2019-05-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03390998 on ClinicalTrials.gov