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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00742014
Other study ID # 1000012265
Secondary ID
Status Terminated
Phase Phase 3
First received
Last updated
Start date August 2008
Est. completion date August 2011

Study information

Verified date April 2016
Source The Hospital for Sick Children
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Terminated
Enrollment 10
Est. completion date August 2011
Est. primary completion date August 2011
Accepts healthy volunteers No
Gender All
Age group 1 Year to 18 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Canada The Hospital for Sick Children Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
The Hospital for Sick Children

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Increase (% change) in endsystolic elastance of the right ventricle from baseline (in comparison to change in endsystolic elastance after inhaled NO) 30 mins after Sildenafil adminsitration
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