Fibrosis and the Fontan

Single-ventricle Clinical Trial

Official title:

Acute Imposition of Fontan Physiology in The Single Ventricle Patient: Effects on Fibrosis, Function and Drug Intervention

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04901975
• Other study ID #: 20-017716
• Secondary ID: 1R01HL149139-01A
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: February 11, 2021
• Est. completion date: June 30, 2024

Study information

• Verified date: February 2024
• Source: Children's Hospital of Philadelphia
• Contact: Mark Fogel, MD
• Phone: 215-590-4040
• Email: fogel[@]chop.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to non-invasively characterize the fibrotic consequences of single ventricle physiology, its possible solution and effect on lymphatics. This project investigates the response to acute imposition of Fontan hemodynamics by examining the interrelationship between liver and cardiac fibrosis/dysfunction and lymphatic congestion along with a pilot trial of the antifibrotic agent, spironolactone, to prevent these consequences and to determine if MRI can discern these differences. The combination of serum biomarkers and MRI form a powerful non-invasive tool in putting together this complicated web of dysfunction.

Description:

Fontan patients, unfortunately, suffer multiple complications such as liver fibrosis, cardiac fibrosis and lymphatic congestion. While investigations describing the clinical state are taking place in older children and young adults, the onset of these complications remains unclear. The knowledge gap this proposal seeks to fill is understanding how early liver and cardiac fibrosis develops as well as lymphatic abnormalities by assessing these before as well as early after imposition of the Fontan circulation. Single ventricle case subjects will be between aged 1 and less than or equal to 6 years of age of either gender, whether single left or right ventricle, who are scheduled to undergo a Fontan operation at the Children's Hospital of Philadelphia (CHOP) and control subjects will be aged between 1 and less than or equal to 6 years of age with normal ventricular function and normal livers who present to CHOP for a clinically indicated MRI. Review of medical records, demographic/social history, physical examination (performed for clinical purposes), administer study drug (spironolactone), blood tests (serum biomarkers), MRI/CMR (including a non-FDA approved MRI sequence), liver assessment, administration of contrast and general anesthesia for case subjects (in some instances, an extension of clinically indicated anesthesia for control and some case subjects approximately 15-20 minutes) as applicable. The difference between enrollment and 1 year after Fontan surgery for a) liver fibrosis measured by Magnetic Resonance Elastography (MRE) and T1 mapping, b) cardiac fibrosis measured by T1 mapping using global extracellular volume (ECV) and c) percentage of myocardial mass which demonstrates delayed enhancement (DE). This is for both non-drug and spironolactone administered groups

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 120
• Est. completion date: June 30, 2024
• Est. primary completion date: March 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Year to 6 Years

Eligibility

Inclusion Criteria:

• Single Ventricle (SV) Patients

Cohort 1 (Observational Group - no study medication):

• Subjects between 1 and = 6 years of age of either gender.
• Either single left or single right ventricle.
• Subjects who are scheduled to undergo a Fontan operation at CHOP.
• Parents signing informed consent. Cohort 1A (formerly part of study drug group who wish continued participation in the

observational group):

• Subjects who were enrolled in this study in Cohort 2 and are either non-compliant with the medication, no longer want to take the medication, or have an AE that requires them to stop the medication, and patient's family would like to continue participation
• Patients were on study medication for 6 weeks or less.
• The principal investigator deems it appropriate for the patient to switch to the observational arm.
• Patients signing the observational informed consent form.

Cohort 1B (observational group - in other studies with intervention):

• Subjects between 1 and =6 years of age of either gender.
• Either single left or single right ventricle.
• Subjects who are planned to undergo a Fontan operation at CHOP.
• Patients in other interventional studies approved by principal investigator.
• Patients signing the observational informed consent form.

Cohort 2 (study drug Group - spironolactone):

• Subjects between 1 and = 6 years of age of either gender.
• Either single left or single right ventricle.
• Subjects who are scheduled to undergo a Fontan operation at CHOP.
• Parents signing informed consent. Controls
• Subjects between 1 and = 6 years of age of either gender
• Subjects with normal ventricular function and normal livers who present to CMR for clinical indications and require anesthesia.
• Receiving contrast for clinical purposes. No control patient will receive contrast for research purposes.
• Parents signing informed consent. Exclusion Criteria: -

Cohort 1 (Observational Group - no study medication):

• Subjects with any condition judged by the patient's physician that would cause this trial to be detrimental to the patient.
• Any contradiction to a sedated CMR (i.e. presence of a pacemaker).
• Patient currently taking spironolactone or eplerenone
• Subjects in any study that would preclude participation in the study by altering results Cohort 1A (formerly part of study drug group who wish continued participation in the

observational group):

• Subjects with any condition judged by the patient's physician that would cause this trial to be detrimental to the patient.
• Any contradiction to a sedated CMR (i.e. presence of a pacemaker).
• Subjects in any study that would preclude participation in the current study.

Cohort 1B (observational group - in other studies with intervention):

• Subjects with any condition judged by the patient's physician that would cause this trial to be detrimental to the patient.
• Any contradiction to a sedated CMR (i.e. presence of a pacemaker).
• Patient currently taking spironolactone or eplerenone
• Subjects in any study that would preclude participation in the current study or studies not approved by principal investigator.

Cohort 2 (Study Drug Group - Spironolactone):

• Subjects with any condition judged by the patient's physician that would cause this trial to be detrimental to the patient.
• Any contradiction to a sedated CMR (i.e. presence of a pacemaker).
• Patient currently taking spironolactone or eplerenone
• Subjects with hyperkalemia or Addison disease;
• Subjects on enalapril or other angiotensin receptor blockers
• Subjects with a history of hypersensitivity to spironolactone suspension or any component of the formulation
• Subjects with a clinically documented diagnosis of severe renal insufficiency (implying estimated glomerular filtration rate (eGFR) <30 mL/minute/1.73 m2).
• Subjects in any study that would preclude participation in the study by altering results Controls
• Any condition judged by the patient's physician that would cause this trial to be detrimental to the patient.
• Any contradiction to a sedated CMR (i.e. presence of a pacemaker).
• Patient currently taking spironolactone, eplerenone or an angiotensin converting the enzyme inhibitor/angiotensin receptor blocker.

Related Conditions & MeSH terms

• Single-ventricle
• Univentricular Heart

Intervention

Drug:
• Spironolactone
Spironolactone is a mild diuretic. Drug dosage will be those used clinically and per the CHOP formulary: 3 mg/kg/day in divided doses every 6-24 hours; the drug will be weight adjusted every ~0.5 kg with a maximum dosage of 200 mg/24 hours. Maximum single dose is 100 mg. Spironolactone, the aldosterone antagonist to be utilized in Specific Aim 2 of this study, is FDA approved, has been on the market for many years and is routinely administered to all types of children with congenital heart disease including SV patients. The choice of which patient this should be administered to is up to the clinician and their patients and therefore, not all SV patients are on this medication.

Locations

Country	Name	City	State
United States	Children's Hospital of Philadelphia	Philadelphia	Pennsylvania

Sponsors (2)

Lead Sponsor	Collaborator
Children's Hospital of Philadelphia	National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Liver elastography by MRE prior to and after Fontan	Measured by MRE for viscoelastic properties of the liver, primarily stiffness	up to 1 year
Primary	Liver elastography by T1rho prior to and after Fontan	Measured by T1rho mapping for further viscoelastic properties of the liver, primarily hepatic fibrosis	up to 1 year
Primary	Heart tissue characterization by T1 mapping prior to and after Fontan	Measured by T1 mapping using global extracellular volume (ECV)	up to 1 year
Primary	Heart tissue characterization prior to and after Fontan	Percentage of myocardial mass which demonstrates delayed enhancement	up to 1 year
Secondary	Serum biomarkers of fibrosis	Serum biomarkers of liver will be assessed to include eg Galectin-3, PIIIP and TGF-beta	up to 1 year
Secondary	Lymphatic dysfunction by MRE prior to and after Fontan	Lymphatic dysfunction will be measured by MRE to find if lesions are present	up to 1 year
Secondary	Lymphatic dysfunction T1rho prior to and after Fontan	Lymphatic dysfunction will be measured by T1rho to find if lesions are present	up to 1 year