Sildenafil for Early Pulmonary Vascular Disease in Scleroderma

Who is this study for? Patients with early pulmonary vascular disease in scleroderma
What treatments are being studied? Sildenafil
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is a Phase II randomized, double-blind, placebo-controlled trial of sildenafil in men and women with Scleroderma with mildly elevated pulmonary pressures (SSc-MEP) to determine whether sildenafil may be an effective treatment for SSc-MEP.

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

• Previous documentation of mean pulmonary artery pressure between 21 and 24 mm Hg with a pulmonary capillary wedge pressure (or left ventricular end-diastolic pressure) ≤ 15 mm Hg within six months before study entry.

• Diagnosis of SSc according to 2013 American College of Rheumatology/ European League Against Rheumatism (ACR/EULAR) classification criteria.

• Pulmonary function tests with forced expiratory volume in one second/forced vital capacity (FEV1/FVC) \>50% AND either a) total lung capacity (TLC) or forced vital capacity (FVC) \> 70% predicted or b) TLC or FVC between 60% and 70% predicted with no more than mild interstitial lung disease on computerized tomography scan of the chest on studies obtained within 6 months of enrollment.

• Ventilation perfusion scan or computed tomography with intravenous contrast (CT angiogram) without evidence of chronic thromboembolism at anytime before study entry.

• Ability to perform six minute walk testing without significant limitations in musculoskeletal function or coordination.

• Informed consent.

Locations
United States
Louisiana
Louisiana State University
NOT_YET_RECRUITING
New Orleans
Maryland
Johns Hopkins
RECRUITING
Baltimore
Contact Information
Primary
Stephen Mathai, MD
smathai4@jhmi.edu
4106146311
Backup
Renee Ofori
rofori2@jhu.edu
410-614-6311
Time Frame
Start Date: 2021-09-20
Estimated Completion Date: 2026-09-01
Participants
Target number of participants: 30
Treatments
Experimental: Sildenafil
Sildenafil 20 mg by mouth three(3) times each day
Placebo_comparator: Placebo
Placebo by mouth three(3) times each day
Related Therapeutic Areas
Sponsors
Collaborators: United States Department of Defense, Louisiana State University Health Sciences Center in New Orleans
Leads: Johns Hopkins University

This content was sourced from clinicaltrials.gov

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