Revatio Portal-Pulmonary Arterial Hypertension Trial

Phase 2

Terminated

• Conditions: Portopulmonary Hypertension
• Interventions: Drug: Placebo; Drug: Sildenafil

• Registration Number: NCT01517854
• Lead Sponsor: University Health Network, Toronto

Brief Summary

The investigators propose the first prospective, double blind, randomized controlled trial of treatment for pulmonary arterial hypertension (PAH) related to underlying portal hypertension. Specifically the investigators will evaluate the potential efficacy and safety of sildenafil (Revatio) in a 16 week blinded, multicentre study.

Detailed Description

PAH is a recognized complication of portal hypertension - termed portal-pulmonary hypertension (PPHTN). In the World Health Organization (WHO) classification PPHTN is categorized as a WHO group 1 condition. This categorization is appropriate as PPHTN shares similar pathological features and clinical presentation and as idiopathic (primary) pulmonary arterial hypertension (PAH). Advances in oral therapies in PAH (idiopathic, connective tissue disease, congenital heart disease) has deferred the need for parenteral therapies, lung transplantation and led to improvements in functional capacity, quality of life and survival. However unlike other forms of PAH, treatment options have not been formally evaluated for PPHTN and there are no approved medical therapies. Patients are unable to pay for medications. Consequently patients continue to endure the natural progression of PAH - a state characterized by progressive right heart failure, disability and death. Furthermore the unacceptable mortality associated with liver transplantation in the presence of hemodynamically significant PAH, leaves them with no therapeutic options. Therefore, new treatment options need to be systematically evaluated.

Study Timeline

• Study First Submitted: 2011-12-14
• Study First Submitted QC: 2012-01-20
• Study First Posted: 2012-01-25
• Study Start: 2012-11-14
• Primary Completion: 2017-10-30
• Study Completion: 2019-05-14
• Status Verified: 2019-09
• Last Update Submitted: 2019-09-25
• Last Update Posted: 2019-09-27

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

• Male and female patients with PPHTN.
• A 6MWD test between 150 m and 450 m.
• A pulmonary vascular resistance (PVR) >250 dyn*sec*cm-5, a mean pulmonary artery pressure (PAPmean) ≥25 mmHg due to portal hypertension, and PCWP ≤ 15 mmHg. Right-heart catheterization results for the definite diagnosis of PH must follow the 2 - 6 week pre-treatment phase and not be older than 6 weeks at study start (will be considered as baseline values).
• Portal hypertension defined either clinically or hemodynamically by the presence of cirrhosis (by ultrasound or biopsy) or portal vein thrombosis / obstruction (proven by portal vein Doppler) and any one of the following within one year of entry into the study: 1) Ascites (on ultrasound of the abdomen); 2) Splenomegaly (on ultrasound of the abdomen); 3) Esophageal or Gastric Varices (proven endoscopically); 4) Hepatic-venous pressure gradient (HVPG) > 12 mmHg.
• Treatment naive patients (with respect to PAH specific medication) and patients. Prior use of sildenafil for erectile dysfunction will be permitted.
• 18 to 75 years of age at Visit 1.
• Patients who are able to understand and follow instructions and who are able to participate in the study for the entire period.
• Patients must have given their written informed consent to participate in the study after having received adequate previous information and prior to any study-specific procedures.

Exclusion Criteria

• Participation in another clinical trial during the preceding 3 months.
• Pregnant women or breast feeding women.
• Patients with a medical disorder, condition, or history of such that would impair the patient's ability to participate or complete this study in the opinion of the investigator or the sponsor.
• Patients with a history of severe allergies or multiple drug allergies.
• Patients with hypersensitivity to the investigational drug or inactive constituents.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo	Placebo	-
Revatio	Sildenafil	-

Primary Outcome Measures

Name	Time	Method
Change from baseline in PVR after 16 weeks of treatment	16 weeks

Secondary Outcome Measures

Name	Time	Method
Death	16 weeks
Hospitalizations	16 weeks
Change from baseline in CAMPHOR and SF-36 measures of quality of life	16 weeks
Complications of liver disease	16 weeks
Renal dysfunction	16 weeks
Desaturation	16 weeks
Change in 6MWD from baseline	16 weeks
Change in Brain Natruretic Peptide (BNP) from baseline	16 weeks
MELD score	16 weeks
Change in baseline WHO functional class	16 weeks
For patients with a PVR>450 dynes/sec/cm5 at baseline, number of patients who have PVR below 350 dynes/sec/cm5 after 16 weeks of study drug will be determined	16 weeks

Trial Locations

Locations (3)

Lawson Health Research Institute (London Health Sciences Centre Research Inc.); 🇨🇦 London, Ontario, Canada

Institut universitaire de cardiologie et de pneumologie de Québec; 🇨🇦 Québec, Canada

University Health Network; 🇨🇦 Toronto, Ontario, Canada