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NCT01909674 · ClinicalTrials.gov registry record · NA

Differences in Efficacy Between Nasal and Oronasal Masks in the Treatment of OSA With CPAP

A NA study of Obstructive Sleep Apnea (OSA), sponsored by Weill Medical College of Cornell University.

Completed
Registry status
NA
Development phase
21
Enrollment target
1
Study location

NCT01909674 is a NA study of Obstructive Sleep Apnea (OSA) that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 21 participants, below the 590-participant average among 12 other Obstructive Sleep Apnea (OSA) trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01909674, a NA study of Obstructive Sleep Apnea (OSA), has completed, sponsored by Weill Medical College of Cornell University.

COMPLETED
Registry status
NA
Development phase
21 participants
Enrollment target
1
Study location

Study Summary

Our group previously conducted a study looking at the performance of three styles of positive airway pressure masks during laboratory treatment studies for obstructive sleep apnea, and we found that patients using a full-mask mask required higher positive airway pressures than patients using nasal or nasal pillows style masks to achieve successful reduction of respiratory events. In the current study we want to randomly assign patients to either nasal or full-face masks and then switch to a different mask (if nasal was originally chosen than the mask will be switched to full-face and vise versa) after 3-weeks of use to see if the number of respiratory events change with the different mask style. We expect the number of respiratory events will increase with the use of full-face masks.

Interventions

  • DEVICE Switch CPAP mask type

Study Locations (1)

New York

  • Weill Cornell Center for Sleep Medicine - New York

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2011-09
Est. Completion 2013-08
Phase NA

What the Registry Record Tells You About NCT01909674

The ClinicalTrials.gov registry entry for NCT01909674 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 590-participant average among 12 other Obstructive Sleep Apnea (OSA) trials with a reported enrollment target (96% lower). The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Obstructive Sleep Apnea (OSA) appearing as the primary indexed condition, and to 1 intervention - of which Switch CPAP mask type is the first listed.

NCT01909674 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT01909674 about?

NCT01909674 is a clinical study titled "Differences in Efficacy Between Nasal and Oronasal Masks in the Treatment of OSA With CPAP". Our group previously conducted a study looking at the performance of three styles of positive airway pressure masks during laboratory treatment studies for obstructive sleep apnea, and we found that patients using a full-mask mask required higher positive airway pressures than patients using nasal o...

What is the current status of trial NCT01909674?

This trial is currently completed. It is a NA study. The enrollment target is 21 participants. The study started on 2011-09. Estimated completion is 2013-08.

What conditions does trial NCT01909674 study?

This clinical trial studies the following conditions: Obstructive Sleep Apnea (OSA).

What interventions are being tested in trial NCT01909674?

The interventions under investigation include: Switch CPAP mask type (DEVICE).

Who is sponsoring clinical trial NCT01909674?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01909674 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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