Effect of Carvedilol on Exercise Performance in Fontan Patients

The University of Texas System (UT)

Status and phase: Completed; Phase 4

Conditions: Single Ventricle; Fontan

Treatments: Drug: Placebo; Drug: Carvedilol

Study type: Interventional

Funder types: Other

Identifiers

NCT02946892

062016-101

Details and patient eligibility

About

This study evaluates the effect of carvedilol in patients who have undergone a Fontan heart operation. All participants will receive carvedilol and placebo for 12 weeks. Exercise tests will be performed at the end of each 12 week period.

Full description

Carvedilol is a well studied heart failure medication in adult heart failure that has been shown to improve outcomes. However, it has not been studied in patients who have had a Fontan heart operation. Study participants will receive either placebo or carvedilol for 12 weeks, at the end of the 12 weeks participants will perform an exercise test. Then study participants will receive treatment with placebo or carvedilol for 12 weeks (opposite of what participants go the first 12 weeks) and will again perform an exercise test.

Enrollment: 26 patients

Sex: All

Ages: 10 to 35 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Informed consent of parent(s) or legal guardian; informed consent or assent of subject as applicable.
2. Male or female children between the ages of 10 and 35 years with congenital heart disease that has been palliated with a Fontan circulation.
3. Ability of perform a maximal exercise test as defined by a respiratory exchange ratio (RER) greater than 1.0 at the time of maximal exercise

Exclusion criteria

1. The use of beta blockers within 2 months of randomization
2. Patients actively listed for transplantation at time of entry into the study or anticipated to undergo heart transplantation, interventional catheterization, or corrective cardiac surgery during the 7 months following entry into the study
3. Sustained or symptomatic ventricular dysrhythmias uncontrolled by drug therapy or the use of an implantable defibrillator, and/or significant cardiac conduction defects, e.g., 2nd degree or 3rd degree AV block, or sick sinus syndrome, unless a functioning pacemaker is in place
4. Uncorrected obstructive or severe regurgitant valve disease, nondilated cardiomyopathy, or significant systemic ventricular outflow obstruction
5. Known renovascular hypertension or evidence of pulmonary hypertension (pulmonary vascular resistance > 6 Wood units) unresponsive to vasodilator agents such as oxygen, nitroprusside, or nitric oxide
6. History or current clinical evidence of moderate-to-severe fixed obstructive pulmonary disease or severe reactive airway diseases (e.g., asthma) requiring hospitalization within the past 2 years or patient currently using long-term inhaled bronchodilators
7. Renal, hepatic, gastrointestinal, or biliary disorder that could impair absorption, metabolism or excretion of orally administered medication
8. Concurrent terminal illness or other severe disease (e.g., active neoplasm) or other significant laboratory value(s) which, in the opinion of the investigator, could preclude participation or survival
9. Endocrine disorders such as primary aldosteronism, pheochromocytoma, hyper- or hypothyroidism, insulin-dependent diabetes mellitus
10. Unwillingness or inability to cooperate, or for the parents or guardians to give consent, or for the child to give assent, or any condition of sufficient severity to impair cooperation in the study
11. Pregnancy or possible pregnancy at time of randomization, or female of child bearing potential who are lactating, or sexually active and not taking adequate contraceptive precautions (e.g., intrauterine device or oral contraceptives for 3 months prior to entry into the study)
12. Use of an investigational drug within 30 days of randomization, or within 5 half-lives of the investigational drug (the longer period will apply)
13. History of drug sensitivity or allergic reaction to alpha-blockers or ß-blockers
14. Use of any of the following medications within two weeks of randomization: MAO inhibitors, Calcium channel blockers, alpha blockers, beta blockers, disopyramide, flecainide, encainide, moricizine, propafenone, sotalol, or beta adrenergic agonists
15. Hospital admission for protein losing enteropathy or plastic bronchitis within 3 months of randomization
16. Active and/or chronic protein losing enteropathy or plastic bronchitis (on inhaled medication to control the plastic bronchitis).
17. Hypoalbuminemia defined as serum albumin <2.0g/dL
18. Renal dysfunction defined as serum creatinine >2.0mg/dL
19. Hepatic dysfunction defined as serum AST and/or ALT> 3 times upper limit of normal (approximately 120 IU/L however, will vary depending on age),
20. Significant anemia or polycythemia defined as hemoglobin >18gm/dL or hemoglobin <7gm/dL
21. Severely elevated serum BNP defined as BNP>300pg/ml

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Quadruple Blind

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26 participants in 2 patient groups

Carvedilol

Experimental group

Description:

Study participants will receive carvedilol for 12 weeks

Treatment:

Drug: Carvedilol

Placebo

Experimental group

Description:

Study participants will receive placebo (sugar pill) for 12 weeks

Treatment:

Drug: Placebo