The Assessment of Right Ventricular Contractility in Response to Sildenafil

NCT ID: NCT00742014

Last Updated: 2021-04-19

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE3
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-08-31
• Study Completion Date: 2011-08-31

Brief Summary

The primary objective of this study is to examine the effects of Sildenafil, administered during cardiac catheterization, on right ventricular contractility in children with pulmonary arterial hypertension.

Detailed Description

The effectiveness of Sildenafil as a pulmonary vasodilator in children with heart disease was first reported in detail during cardiac catheterization and postoperatively in 2003. It is now used frequently for long-term treatment of children with pulmonary arterial hypertension at The Hospital for Sick Children and it is now a routine part of the hospital's testing protocol for all patients being evaluated for pulmonary hypertension in the cardiac catheterization laboratory.

The beneficial effects of Sildenafil in pulmonary hypertension are thought to result predominantly from relative vasodilatory and antiproliferative effects on the pulmonary vasculature. On the basis of early data showing lack of significant PDE5 expression in the normal heart, PDE5 was thought to be expressed in the coronary vessels but not in the human myocardium. Very recently, it was reported for the first time that PDE5 is markedly upregulated in hypertrophied right ventricular myocardium in humans and that in the rat PDE5 inhibition with Sildenafil increases contractility in hypertrophied right ventricular myocardium but not in normal right ventricle, which lacks PDE5 expression. The assessment of right ventricular contractility in humans is a challenge, but we have developed several techniques that are recognized as 'state of the art' assessment of right ventricular function.

The purpose of this study is to examine the effects of Sildenafil, which is routinely administered during cardiac catheterization to assess pulmonary vascular resistance, on right ventricular contractility in children with pulmonary arterial hypertension.

Conditions

Hypertension

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

1

Group Type: EXPERIMENTAL

Sildenafil

Intervention Type: DRUG

One oral dose of Sildenafil (0.5 mg/kg) will be administered nia a nasogastric tube

Interventions

Sildenafil

One oral dose of Sildenafil (0.5 mg/kg) will be administered nia a nasogastric tube

Intervention Type: DRUG

Other Intervention Names

Viagra

Eligibility Criteria

Inclusion Criteria

• Significant pulmonary arterial hypertension (mean pulmonary artery pressure > 25 mm Hg)
• Patients aged 4-18 years
• Routine cardiac catheterization clinically indicated for deciding therapeutic treatment
• Informed assent/consent from patient/parent

Exclusion Criteria

• Suprasystemic pulmonary artery pressures
• Evidence of right heart failure
• History of ventricular arrhythmia
• Known vascular access arrhythmia
• Contraindication to Sildenafil
• Concurrent inotropic / PDE administration
• Other medical, psychological or social circumstances which complicate a regular participation in the study, and/or increase the risk for the patients themselves
• No consent/assent
• Pregnancy or unwillingness to comply with contraceptive advice

• Minimum Eligible Age: 1 Year
• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

The Hospital for Sick Children

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Andrew Redington, MD

Role: PRINCIPAL_INVESTIGATOR

The Hospital for Sick Children

Locations

The Hospital for Sick Children

Toronto, Ontario, Canada

Countries

Canada

Other Identifiers

1000012265

Identifier Type: -

Identifier Source: org_study_id