MedPath

A study to compare how well patients do with treatment after undergoing full monitoring in a sleep laboratory versus simplified sleep study recordings to test for possible obstructive sleep apnea

Not Applicable
Completed
Conditions
Obstructive sleep apnea
Respiratory - Sleep apnoea
Registration Number
ACTRN12611000926932
Lead Sponsor
Australasian Sleep Trials Network
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
400
Inclusion Criteria

1) Patients must be aged between 25-80 years. 2) Are referred to a sleep disorders centre for investigation of suspected OSA. 3) Report at least 2 of the following symptoms: snoring, witnessed apneas and/or excessive daytime sleepiness.

Exclusion Criteria

1) Have had a previous sleep study
2) Referral for a non-respiratory sleep disorder
3) Have a severe psychiatric disorder or cognitive impairment that may affect the ability of the subject to comply with the study protocol
4) Suffer from neuromuscular disease, severe chronic obstructive (FEV1/FVC <70% and FEV1 <50% predicted) or restrictive (TLC <70% predicted) pulmonary disease, or require supplemental oxygen
6) Have unstable cardiovascular disease or cardiac failure (ie New York Heart Association categories III-IV)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath