Clinical Study for the BONGO Device in the Treatment of Obstructive Sleep Apnea (OSA)

NCT02878590 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2019-02-19

Study results available
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Summary

Prospective, non-randomized, open label study

Conditions

Interventions

DEVICE

BONGO DEVICE

A device to be used for the treatment of mild to moderate obstructive sleep apnea

Sponsors & Collaborators

  • RVW Clinical Consulting

    collaborator INDUSTRY
  • InnoMed Healthscience Inc.

    lead INDUSTRY

Principal Investigators

  • jerrold kram, MD · California Center for Sleep Disorders

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2017-11-30
Completion
2017-11-30

Countries

  • United States

Study Locations

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Entities

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 NCT02878590 on ClinicalTrials.gov