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Clinical Trial Summary

There are currently very few proven pharmacologic options available for these patients. The recent discovery of transient receptor potential vanilloid (TRPV) channels, particularly TRPV2 channels, in the cardiovascular system is promising as a potential pathway for pharmacologic intervention for Fontan patients. Probenecid, a drug best known as a treatment for gout or as a penicillin adjunct, acts as a TRPV2 agonist and has recently become the subject of study as a model therapy for the treatment of cardiomyopathy due to its positive inotropic and lusitropic effects. The purpose of this pilot study is to determine if probenecid will improve magnetic resonance (MRI) parameters of systolic and/or diastolic dysfunction as well as associated symptoms in patients with a Fontan circulation. The investigators will quantitatively assess functional improvement with pre- and post-treatment cardiopulmonary exercise testing.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03965351
Study type Interventional
Source Children's Hospital Medical Center, Cincinnati
Contact
Status Completed
Phase Phase 4
Start date March 21, 2017
Completion date December 31, 2020

See also
  Status Clinical Trial Phase
Completed NCT02946892 - Effect of Carvedilol on Exercise Performance in Fontan Patients Phase 4
Withdrawn NCT01607983 - Effects of Pulmonary Vasodilation Upon VA Coupling in Fontan Patients Phase 3
Completed NCT04297241 - Nitrate Effect on Exercise Capacitance Phase 2
Not yet recruiting NCT04288596 - Canadian Adult Congenital Heart Disease Intervention Registry