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Effects From a Mandibular Repositioning Appliance in Patients With Obstructive Sleep Apnea and Snoring

NCT00477009 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 96

Last updated 2013-01-18

No results posted yet for this study

Summary

The purpose of this study is to evaluate effects from a mandibular repositioning appliance on obstructive sleep apneas, symptoms, blood pressure and markers of stress, inflammation and cardiovascular health in patients with mild to moderate obstructive sleep apnea/hypopnea syndrome and in patients with symptomatic snoring.

Conditions

  • Sleep Apnea Syndromes
  • Snoring
  • Disorders of Excessive Somnolence

Interventions

DEVICE

Mandibular repositioning appliance, adjustable

Comparison between mandibular repositioning appliance for nightly use and a placebo device regarding effects on sleep apneas and daytime symptoms as well as blood pressure and markers of oxidative stress and sleepiness.

Sponsors & Collaborators

  • The Swedish Research Council

    collaborator OTHER_GOV

  • Umeå University

    lead OTHER

Principal Investigators

  • Marie Marklund · Umeå University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-05-31
Primary Completion
2011-12-31
Completion
2011-12-31

Countries

  • Sweden

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 NCT00477009 on ClinicalTrials.gov