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Efficacy of Sildenafil in Severe Pulmonary Hypertension Secondary to Rheumatic Chronic Valvular Disease: A Double-Blinded Placebo Randomized Control Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

Pulmonary hypertension secondary to left heart disease is associated with increased morbidity and mortality, particularly in patients with rheumatic chronic valvular heart disease, which remains highly prevalent in low- and middle-income countries. These patients often present late with severe pulmonary hypertension, limiting surgical options and worsening outcomes. Sildenafil, a phosphodiesterase-5 inhibitor, has demonstrated benefit in various forms of pulmonary hypertension; however, its role in pulmonary hypertension secondary to rheumatic valvular disease remains inadequately studied. This double-blind, placebo-controlled randomized clinical trial aims to evaluate the efficacy and safety of sildenafil as an adjunct to standard medical therapy in patients with severe pulmonary hypertension due to rheumatic chronic valvular heart disease. Eligible participants will be randomized in a 1:1 ratio to receive either sildenafil (25 mg three times daily) or placebo for six weeks. The primary outcome is change in six-minute walk distance, while secondary outcomes include changes in right ventricular function and dimensions, systolic pulmonary artery pressure, NYHA functional class, and hospitalization rates. The study seeks to generate evidence to support medical optimization and bridging therapy in this high-risk population awaiting definitive surgical intervention.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient with diagnosed rheumatic valvular heart disease

• Age between 18-\> 80 years

• Severe pulmonary hypertension

Locations
Other Locations
Pakistan
Sindh Institute of Cardiovascular Diseases
RECRUITING
Hyderābād
Contact Information
Primary
Dr Aamir Khuwaja
khuwaja.aamir91@gmail.com
03323594539
Backup
Dr Raheela Khowaja
drraheela.allahbux@gmail.com
03312273977
Time Frame
Start Date: 2025-08-01
Estimated Completion Date: 2026-06
Participants
Target number of participants: 100
Treatments
Experimental: Intervention group
Participants receive oral sildenafil 25 mg three times daily for 6 weeks in addition to standard guideline-directed medical therapy for rheumatic chronic valvular heart disease and associated conditions.
Placebo_comparator: Placebo Group
Participants receive matching placebo three times daily for 6 weeks in addition to standard guideline-directed medical therapy.
Sponsors
Collaborators: National Institute of Cardiovascular Diseases
Leads: Sindh Institute of Cardiovascular Diseases

This content was sourced from clinicaltrials.gov