Status:

COMPLETED

A Randomized Study to Compare Polysomnography With Overnight Home Oximetry and Auto - CPAP for Sleep Apnea

Lead Sponsor:

University of British Columbia

Conditions:

Obstructive Sleep Apnea

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

This study will look at an alternative new pathway for diagnosis and treatment based on simple procedures in the patient's own home compared with the current conventional laboratory based pathway. The...

Detailed Description

The research question we are exploring is whether the conventional approach is better in terms of successful treatment, compliance with treatment, and quality of life. There will be 2 arms to the stud...

Eligibility Criteria

Inclusion

  • Age \> 18 years
  • Residence in the Lower Mainland
  • History and physical examination findings compatible with OSAHS
  • Normal spirometry. (This is necessary to avoid decreased specificity of overnight oximetry attributable to underlying lung disease)
  • Epworth Sleepiness Scale \> 10

Exclusion

  • Age \< 18 years
  • Pregnancy
  • Other known disorders that cause daytime sleepiness
  • Requiring sedative/hypnotic medications
  • Psychiatric disorder
  • Life threatening co-morbidity e.g. chronic lung disease, coronary artery disease - unstable angina, recent myocardial infarction, heart failure, seizure disorder, and previous motor vehicle accident attributed to hypersomnolence
  • Language barrier
  • Inability to give informed consent
  • Contraindication to nasal CPAP therapy
  • Previous treatment of OSAHS with nasal CPAP, oral appliance therapy or corrective upper airway surgery.

Key Trial Info

Start Date :

Trial Type :

INTERVENTIONAL

End Date :

December 1 2004

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT00254059

End Date

December 1 2004

Last Update

November 15 2005

Active Locations (1)

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Vancouver Coastal Health Research Institute, Respiratory Division

Vancouver, British Columbia, Canada