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Study of Nasal Airflow Pressure Optimization to Resolve Excessive Snoring

NCT01949584 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26

Last updated 2015-03-24

No results posted yet for this study

Summary

This is a prospective, interventional, study in which patients with a history of habitual snoring to determine whether low pressure nasal continuous airway pressure can reduce the frequency, duration or intensity of snoring in subjects with mild to moderate snoring who do not have Obstructive Sleep Apnea (OSA).

Conditions

  • Snoring

Interventions

DEVICE

nasal continuous positive airway pressure less than or equal to 6 cm H2O

Low level continuous positive airway pressure delivered during sleep.

Sponsors & Collaborators

  • Johns Hopkins University

    collaborator OTHER

  • Doctors Community Hospital

    collaborator UNKNOWN

  • NeuroTrials Research, Inc.

    collaborator OTHER

  • inSleep Technologies, LLC

    lead INDUSTRY

Principal Investigators

  • Michael Lauk · inSleep Tech

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-08-31
Primary Completion
2014-07-31
Completion
2014-12-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01949584 on ClinicalTrials.gov