drugset / Trial / NCT00302211

The "VISION" Trial: Ventavis Inhalation With Sildenafil to Improve and Optimize Pulmonary Arterial Hypertension

NCT00302211

Phase 3 Terminated 67 enrolled Actelion
RandomizedFactorialDouble-blindTreatment

Summary

The purpose of this multi-center international trial is to evaluate the safety and effectiveness of adding iloprost or placebo (an inactive substance that contains no active study drug) to sildenafil therapy for pulmonary arterial hypertension (PAH). The study will also examine whether patients on sildenafil can reduce the number of iloprost inhalations from the approved 6 doses per day to 4 doses per day.

Timeline

Start
2006-02-01
Primary completion
2007-12-01
Completion
2008-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Iloprost Other / unclassified 5 ug Inhaled
Background Bosentan Other / unclassified 62.5 mg Oral
Background Bosentan Other / unclassified 125 mg Oral
Background Sildenafil Unknown 60 mg Oral
Background Sildenafil Unknown 300 mg Oral