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Clinical Study to Determine Safety and Effectiveness of KEEPASLEEP Device in Simple Snorers.

NCT00211627 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2005-09-21

No results posted yet for this study

Summary

Study to demonstrate the safety and effectiveness of a new oral enhanced airway device to treat simple snoring.

Conditions

  • Snoring
  • Sleep Apnea Syndromes

Interventions

DEVICE

KEEPASLEEP enhanced breathing device

Sponsors & Collaborators

  • Miller, Chipp St. Kevin, M.D.

    lead OTHER

Principal Investigators

  • Chipp K. Miller, M.D. · St. Johns Health Center

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2004-06-30
Completion
2006-06-30

Countries

  • United States

Study Locations

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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 NCT00211627 on ClinicalTrials.gov