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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 29 July 2022
Main ID:  NCT01457781
Date of registration: 12/10/2011
Prospective Registration: Yes
Primary sponsor: Bellerophon Pulse Technologies
Public title: Inhaled Nitric Oxide/INOpulse DS for Pulmonary Arterial Hypertension (PAH) PAH
Scientific title: A Phase 2, Placebo Controlled, Double-Blind, Randomized, Clinical Study to Determine Safety, Tolerability and Efficacy of Pulsed, Inhaled Nitric Oxide (iNO) Versus Placebo as Add-On Therapy in Symptomatic Subjects With Pulmonary Arterial Hypertension (PAH)
Date of first enrolment: April 2012
Target sample size: 80
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT01457781
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Crossover Assignment. Primary purpose: Treatment. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).  
Phase:  Phase 2
Countries of recruitment
Canada United States
Contacts
Name:     Stephen Haworth, MB, MRCP
Address: 
Telephone:
Email:
Affiliation:  Bellerophon Therapeutics (consultant)
Key inclusion & exclusion criteria
Health Condition(s) or Problem(s) studied
Intervention(s)
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Secondary Sponsor(s)
Ethics review
Results
Results available:
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