Clinical Trials Directory

Trials / Completed

CompletedNCT01247116

First-line Bosentan and Sildenafil Combination Therapy for Pulmonary Arterial Hypertension

First-line Bosentan and Sildenafil Combination Therapy for Pulmonary Arterial Hypertension: A Safety and Efficacy Pilot Study

Status
Completed
Phase
Study type
Observational
Enrollment
12 (actual)
Sponsor
University of Calgary · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the strategy of initiating double oral combination therapy with bosentan and sildenafil at the time of diagnosis of pulmonary arterial hypertension (PAH) in a preliminary way.

Detailed description

Current treatment paradigms for PAH suggest adopting goals of therapy with relatively objective parameters such as 6 minute walk distance to determine when to add a second oral agent (1). This often entails observing deterioration in the patient on a single agent before instituting the second one. This strategy could be problematic, as patients may never recover the function lost due to progressive PAH (2). In addition, given the malignant nature of the clinical course of PAH in many cases and the nature of the underlying proliferative vasculopathy, some have argued that altering this paradigm to resemble that used in cancer chemotherapy may be more appropriate (3). That is, "induction" therapy at diagnosis with multiple agents followed by a maintenance phase of treatment might offer significant benefits to the patient. This open-label pilot study is the first to investigate the potential efficacy and safety of a first-line combination strategy in consecutive patients with PAH in contrast to the "add-on" strategy for combination therapy. It will serve as the basis on which to consider larger, multicenter investigations of this strategy. 1. Hoeper M, et al. Eur Respir J. 2005 Nov;26(5):858-63. 2. Halpern SD, et al. Proc Am Thorac Soc. 2008 Jul 15;5(5):631-5. 3. Provencher S, et al. Chest. 2005 Dec;128(6 Suppl):622S-628S.

Conditions

Timeline

Start date
2009-12-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2010-11-24
Last updated
2018-06-12

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01247116. Inclusion in this directory is not an endorsement.