CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 57 enrolled
Drug / intervention
F&P Seal Improvement Projectdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03142438
NCT03142438N/ACompleted
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The Evaluation of a Full Face and Nasal Mask for the Treatment of Obstructive Sleep Apnea

Fisher and Paykel Healthcare·interventional·Posted May 5, 2017·Updated Jul 14, 2021

In Brief

A clinical study evaluating F&P Seal Improvement Project for Obstructive Sleep Apnea. Completed, enrolled 57 participants across 1 site.

Detailed Summary

This investigation is a prospective, non randomized, non blinded study. This investigation is designed to evaluate the performance, comfort and ease of use with the F\&P trial full face and nasal mask amongst Obstructive Sleep Apnea (OSA) patients. Up to 70 OSA patients will be recruited from the North Texas Lung and Sleep Clinic (NTLSC) database

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsObstructive Sleep Apnea
CountriesUnited States
CollaboratorsNorth Texas Lung & Sleep Clinic

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedMay 5, 2017
Enrollment StartMay 30, 2017
Primary CompletionJun 23, 2017
TodayJul 2, 2026
Enrollment to primary: 23 daysPosted 9.2 years ago

Interventions

F&P Seal Improvement Projectdevice

Participants will be placed on this arm for a total 14 ± 4 days from Visit 1. Participants will be using the trial full face or nasal mask during this treatment arm.