RecruitingACTRN12605000441617

Use of a CO2 clamp and or CPAP to stabilize respiration in patients with combined central and obstructive sleep apnoea

Sponsor

Dr R Ratnavadivel, Adelaide Institute for Sleep Health, Daws Rd, Daw Park SA 5041

Enrollment

10 participants

Start Date

Mar 1, 2005

Study Type

Interventional

Conditions

Central and Obstructive sleep apnoea

Eligibility

Sex: Both males and females

Inclusion Criteria1

Presence of central and or obstructive sleep apnoea. Clinically stable 1 month. Willing and competent to sign consent.

Exclusion Criteria1

Significant psychiatric disease. Claustrophobia. inability to tolerate CPAP via mask overnight.

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Interventions

To test efficacy of device under development in treating combined central and obstructive sleep apnoea as compared to conventional CPAP as control. The subject will undergo one night polysomnography

To test efficacy of device under development in treating combined central and obstructive sleep apnoea as compared to conventional CPAP as control. The subject will undergo one night polysomnography whilst using device and one night polysomnography with CPAP (control) in randomized order 1 week apart. The subject will be requested to wear CPAP at night for one week at home prior to each study night to acclimatize to positive airway pressure and mask.

Locations(1)

Australia

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ACTRN12605000441617