Trials / Completed
CompletedNCT00313222
Bosentan Effects in Inoperable Forms of Chronic Thromboembolic Pulmonary Hypertension
Prospective, Randomized, Placebo-controlled, Double-blind, Multicenter, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of Bosentan in Patients With Inoperable Chronic Thromboembolic Pulmonary Hypertension (CTEPH)
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 157 (actual)
- Sponsor
- Actelion · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The present trial investigates a possible use of oral bosentan, which is currently approved for the treatment of symptoms of pulmonary arterial hypertension (PAH), to patients suffering from inoperable chronic thromboembolic pulmonary hypertension (CTEPH) because of (i) peripheral localization of thrombotic material or (ii) persistent or recurrent pulmonary hypertension after pulmonary endarterectomy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | bosentan |
Timeline
- Start date
- 2005-10-01
- Primary completion
- 2007-02-01
- Completion
- 2007-03-01
- First posted
- 2006-04-12
- Last updated
- 2025-02-03
Source: ClinicalTrials.gov record NCT00313222. Inclusion in this directory is not an endorsement.