Ignite Creation Date:
2024-05-05 @ 10:23 PM
Last Modification Date:
2024-10-26 @ 10:17 AM
Study NCT ID:
NCT01092559
Status:
COMPLETED
Last Update Posted:
2013-06-04
First Post:
2010-02-16
Brief Title:
Pilot Study Evaluating the Safety and Performance of the GeNO NITROsyl Delivery System for Inhaled Nitric Oxide
Sponsor:
Geno LLC
Organization:
Geno LLC
Study Overview
Official Title:
An Open Label Pilot Study Evaluating Preliminary Safety and Performance of the GeNO Nitrosyl Delivery System
Status:
COMPLETED
Status Verified Date:
2013-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PILOT
Brief Summary:
This is an open label phase 2 pilot study designed to evaluate the safety tolerability and device performance of the GeNO nitrosyl delivery system during right heart catheterization RHC in participants with pulmonary arterial hypertension PAH All participants will receive inhaled nitric oxide in oxygen or nitric oxide in air delivered by nasal cannula Hemodynamics clinical laboratory and clinical assessment data will be collected on all participants to evaluate safety
Detailed Description:
TREATMENTFOLLOW-UP
Participants meeting eligibility criteria will receive open label nitric oxide at 80 ppm via a nasal cannula Hemodynamic clinical laboratory and clinical assessment data will be collected at baseline after 15 minutes of inhaled nitric oxide administration post RHC procedure and at hospital discharge Day 5 - 3 post RHC telephone contact to assess general health status
Participants meeting eligibility criteria will receive open label nitric oxide at 80 ppm via a nasal cannula Hemodynamic clinical laboratory and clinical assessment data will be collected at baseline after 15 minutes of inhaled nitric oxide administration post RHC procedure and at hospital discharge Day 5 - 3 post RHC telephone contact to assess general health status
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None