Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00780728

Study Evaluating the Addition of Sildenafil to Bosentan Therapy in Pulmonary Arterial Hypertension

Addition of Sildenafil to Bosentan Monotherapy in Patients With Pulmonary Arterial Hypertension (PAH)

Status
Withdrawn
Phase
Phase 3
Study type
Interventional
Enrollment
Sponsor
University Health Network, Toronto · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers

Summary

This study will examine the effects of add-on sildenafil to bosentan monotherapy in patients with Pulmonary Arterial Hypertension. Patients on bosentan monotherapy will be followed every 6 months to assess if they have met the pre-defined treatment goals. If a patient fails to achieve these treatment goals or fails to maintain them, sildenafil will be added to their existing bosentan monotherapy. Patients will be assessed 6 months after start of combination therapy for changes in 6MWT, Borg dyspnea scale, WHO functional class, quality of life.

Conditions

Interventions

TypeNameDescription
DRUGSildenafil

Timeline

First posted
2008-10-28
Last updated
2009-11-13

Source: ClinicalTrials.gov record NCT00780728. Inclusion in this directory is not an endorsement.

Study Evaluating the Addition of Sildenafil to Bosentan Therapy in Pulmonary Arterial Hypertension (NCT00780728) · Clinical Trials Directory