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Clinical Trials/ACTRN12605000415606
ACTRN12605000415606
Recruiting
Not Applicable

The effect of inspiratory duration and chinstrap during non-invasive ventilation: Effects on sleep quality and gas exchange in subjects with nocturnal hypoventilation

ResMed Ltd0 sites25 target enrollmentSeptember 15, 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
ResMed Ltd
Enrollment
25
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 15, 2005
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
ResMed Ltd

Eligibility Criteria

Inclusion Criteria

  • Patients with documented nocturnal hypoventilation from any cause. Using non\-invasive ventilation chronically at home. Be using a bilevel pressure preset ventilator at home in the spontaneous mode. Be using a nasal interface with NIV. Preferably to be using NIV without the use of supplemental oxygen. To be included in the study, subjects will: 1\. Have to have sustained improvements in gas exchange and symptomatolgy. 2\. Be compliant with non\-invasive ventilation at home (using \>5hrs per night). 3\. Able to attend the sleep laboratory on 3 nights within the trial period (ie 6 nights).

Exclusion Criteria

  • Subjects will be excluded from the study where: 1\. Their is limited upper limb movement which would prevent or limit the removal of the nasal mask. 2\. Significant psychiatric or psychological conditions exist which are likely to prevent accurate reporting in regard to the comfort of therapy. 3\. A history of acute respiratory illness within the last month. 4\. The taking of any hypnotic or anti\-depressant medication.

Outcomes

Primary Outcomes

Not specified

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