Study:
A Randomized, Double-blind, Placebo-controlled, Multicenter Study to Assess the Efficacy, Safety, and Tolerability of Bosentan in Patients With Mildly Symptomatic Pulmonary Arterial Hypertension (PAH)
Rationale:
n/a
Purpose:
The present trial investigates a possible use of oral bosentan, which is currently approved
for the treatment of symptoms of pulmonary arterial hypertension (PAH) Class III and IV, to
patients suffering from PAH Class II.
Study Status: Completed
Recruiting:
n/a
| Condition |
Intervention |
Phase |
|
Pulmonary Hypertension |
Drug: bosentan Drug: placebo |
Phase 3 |
Verified by
Actelion
August, 2011
Sponsored by: Actelion
Information provided by: Actelion
ClinicalTrials.gov identifier: NCT00091715
Study Type: Interventional
Study Design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Cleveland Clinic Foundation
Cleveland, Ohio 44195
United States
n/a