Myocardial Perfusion and Scarring in Adults With Congenital Heart Disease

Completed

• Conditions: Cardiac Disease

• Registration Number: NCT02861365
• Lead Sponsor: Children's National Research Institute

Brief Summary

This is a study of the perfusion of the myocardium in adults with specific forms of repaired congenital heart disease using established cardiac MRI techniques and correlating perfusion with clinical outcomes.

Detailed Description

This is a study of the perfusion of the myocardium in adults with specific forms of repaired congenital heart disease using established cardiac MRI techniques and correlating perfusion with clinical outcomes. The investigators objectives are to examine myocardial perfusion both during stress and at rest in adults with repaired or palliated congenital heart disease as well as quantify ventricular function, regional myocardial strain and evidence of myocardial fibrosis with quantitative measures of myocardial perfusion. The specific aim of this study is to understand whether clinical subendocardial perfusion defects contribute to the late decompensation of adult subjects that have single ventricle physiology and adult subjects that have a systemic right ventricle.

Study Timeline

• Study Start: 2013-07
• Study First Submitted: 2016-07-12
• Study First Submitted QC: 2016-08-05
• Study First Posted: 2016-08-10
• Primary Completion: 2020-01-18
• Study Completion: 2020-01-18
• Status Verified: 2021-03
• Last Update Submitted: 2021-03-04
• Last Update Posted: 2021-03-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

• Subjects 18 years of age or older
• All defects that have a right ventricle that supports the systemic circulation
• All defects with a functional single ventricle
• Written informed consent

Exclusion Criteria

• Subjects with a contraindication to magnetic resonance imaging (MRI) scanning will be excluded. These contraindications include subjects with the following devices:

  • Central nervous system aneurysm clips
  • Implanted neural stimulator
  • Implanted cardiac pacemaker or defibrillator
  • Cochlear implant
  • Ocular foreign body (e.g. metal shavings)
  • Implanted Insulin pump
  • Metal shrapnel or bullet

• Severe heart damage that makes it difficult to breathe while lying flat

• Pregnant women (Women of childbearing potential who are uncertain as to whether they are pregnant will be required to have a screening urine or blood pregnancy test)

• Subjects with active symptoms of myocardial ischemia occurring despite maximally tolerated doses of oral antianginal therapy and intravenous nitroglycerin

• Furthermore, the following subject groups will be excluded from studies involving the administration of MRI contrast agents:

  • lactating women unless they are willing to discard breast milk for 24 hours after receiving gadolinium
  • renal disease (estimated glomerular filtration rate [eGFR] < 30 ml/min/1.73 m2 body surface area)

The eGFR will be used to estimate renal function if reported by the laboratory. Otherwise, estimated glomerular filtration rate (eGFR) can be based on the Modification of Diet in Renal Disease (MDRD) study equation (see below) in subjects with stable renal function. This formula is not applicable to subjects with acute renal insufficiency:

eGFR (ml/min/1.73 m2) = 175 x (serum creatinine)-1.154 x (age)-0.203 x 0.742 (if the subject is female) x 1.212 (if the subject is black)

Additional Exclusion Criteria for Vasodilator Stress MRI:

• Myocardial infarction within 24 hours
• Uncontrolled heart failure
• Uncontrolled asthma or emphysema
• Ventricular arrhythmia (sustained ventricular arrhythmia at the time of MR scan)
• Second degree heart block or higher

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Myocardial Ischemia measuring coronary perfusion reserve.	5 years	Compare quantitative myocardial perfusion at stress and rest with measures of systolic and diastolic function in exams performed in close temporal proximity.
Myocardial Ischemia measuring ejection fraction.	5 years	Compare the extent of myocardial ischemia through ejection fraction measurement of the systemic ventricle.
Myocardial Ischemia measuring heart inflow Doppler.	5 years	Compare heart inflow Doppler of the systemic atrioventricular valve to understand the extent of myocardial ischemia.

Secondary Outcome Measures

Name	Time	Method
Scarring and fibrosis by measuring Late Gadolinium Enhancement results.	5 years	Directly compare the extent of myocardial scarring/fibrosis with echo-derived measures of systolic and diastolic function.
Scarring and fibrosis by measuring systolic and diastolic function.	5 years	Compare the extent of myocardial scarring/fibrosis with echo-derived measures of systolic and diastolic function.
Comparison of MRI measurements with blood test.	5 years	Number of participants with predictable future heart failure symptom will be assessed by comparing all cardiac MRI exam measurements with blood test.
Comparison of MRI measurements with walk test.	5 years	Number of participants with predictable future heart failure symptom will be assessed by comparing all cardiac MRI exam measurements with walk test.
Comparison of MRI measurements with NY Heart Association class	5 years	Number of participants with predictable future heart failure symptom will be assessed by comparing all cardiac MRI exam measurements with NY Heart Association class.

Trial Locations

Locations (1)

Children's National Health System; 🇺🇸 Washington, District of Columbia, United States