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A Study of SCAD Using Stress Contrast Echocardiography

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Mayo Clinic

Status

Enrolling

Conditions

Spontaneous Coronary Artery Dissection

Treatments

Procedure: Stress Echocardiography with Contrast

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT07178509
1K23HL155506 (U.S. NIH Grant/Contract)
24-002318

Details and patient eligibility

About

This study aims to fill knowledge gaps regarding microvascular perfusion and pressor response to stress among patients with history of spontaneous coronary artery dissection (SCAD) using stress contrast echocardiography.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult >18 years old
  • Patient has a history of spontaneous coronary artery dissection (SCAD) OR patient is healthy with no significant medical history

Exclusion criteria

  • Unable to give consent
  • Allergic or have a history of adverse reaction to dobutamine, the Definity® ultrasound enhancing agent, or atropine.
  • Has a known or suspected hypersensitivity to perflutren and therefore cannot be given Definity®.
  • Pregnant.
  • Unable to interrupt breastfeeding.
  • Within 3 months of a heart attack.
  • Severe aortic stenosis.
  • Severe, uncontrolled hypertension (>200/110 mmHg at baseline).

Trial design

50 participants in 2 patient groups

Spontaneous coronary artery dissection (SCAD)
Description:
Subject has a history of spontaneous coronary artery dissection (SCAD)
Treatment:
Procedure: Stress Echocardiography with Contrast
Healthy Subjects
Description:
Subjects are healthy with no significant medical history
Treatment:
Procedure: Stress Echocardiography with Contrast

Trial contacts and locations

1

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Central trial contact

Pamela Engrav

Data sourced from clinicaltrials.gov

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