Status:

COMPLETED

Real Time Myocardial Contrast Echocardiography and Dobutamine Stress Perfusion Magnetic Resonance Imaging

Lead Sponsor:

University of Nebraska

Conditions:

Kawasaki Disease

Heart Disease

Eligibility:

All Genders

12-50 years

Brief Summary

The present study is designed to: 1. investigate the safety and efficacy of Real time myocardial echocardiography (RT-MCE) in adolescents and adults ages 12-50 with congenital and acquired congenital...

Detailed Description

Individuals will be identified from the cardiology database and consented during their routine follow up visits. Exercise stress, transthoracic echocardiography and cardiac MR are part of standard med...

Eligibility Criteria

Inclusion

  • • Age between 12 years and 50 years.
  • Male or female.
  • History of repaired congenital heart disease including atrial septal defects, aortic valve disease, tetralogy of fallot, transposition of great arteries and anomalous left coronary artery from pulmonary artery.
  • History of sequelae of heart disease acquired as an infant or child, including Kawasaki disease and coronary ectasia, and patients post anthracycline chemotherapy.
  • Ability to perform Supine bicycle stress with contrast echocardiography as determined by primary cardiologist and/or Dr. Shelby Kutty.
  • Ability to perform CMR with dobutamine stress as determined by the patients primary cardiologist and/or Dr. Shelby Kutty
  • Signed informed consent and assent as applicable.

Exclusion

  • • Atrial or ventricular arrythmias that cannot be controlled to heart rates \< 70/min
  • Intracardiac shunts
  • Known hypersensitivity to perflutren
  • Known hypersensitivity to Dobutamine
  • Congestive heart failure in NYHA class II, III or IV
  • Claustrophobia or any other reason patient is unable to perform CMR (i.e. ferromagnetic implants causing significant artifact that alters image quality, presence of pacemaker, AICD, etc.)
  • Pregnant or possibly pregnant (based on history/information obtained from the patient) or breast feeding

Key Trial Info

Start Date :

April 1 2009

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

March 1 2019

Estimated Enrollment :

124 Patients enrolled

Trial Details

Trial ID

NCT00861848

Start Date

April 1 2009

End Date

March 1 2019

Last Update

September 25 2023

Active Locations (1)

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1

University of Nebraska Medical Center

Omaha, Nebraska, United States, 68198