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NCT01517854: RePo1

Revatio Portal-Pulmonary Arterial Hypertension Trial

Terminated Phase 2 Last updated 27 September 2019
What this trial tests

Phase 2 trial testing Sildenafil in Portopulmonary Hypertension in 12 participants. Terminated before completion.

Timeline
14 November 2012
Primary endpoint
30 October 2017
14 May 2019

Quick facts

Lead sponsorUniversity Health Network, Toronto
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment12
Start date14 November 2012
Primary completion30 October 2017
Estimated completion14 May 2019
Sites3 locations across Canada

Drugs / interventions tested

Conditions studied

Sponsor

University Health Network, Toronto

Who can join

Adults 18 to 75, any sex, with Portopulmonary Hypertension. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Sildenafil

Trials testing the same drug.

Other University Health Network, Toronto trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01517854.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing