None listed
Conditions
Interventions
Participants will be randomised to receive either a conventional humidifier or a novel humidifier (a humidifier that is capable of delivering a higher level of humidity than is typically delivered by a conventional humidifier.) for 4 weeks.
At the end of 4 weeks participants will be swapped to the alternative humidifier for a further 4 weeks.
Duration: 8 weeks (2 4-week treatment arms)
Patient compliance and satisfaction with their treatment will be assessed.
Sponsors
Fisher and Paykel Healthcare
Study design
Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No
Inclusion criteria
1. RDI > 15
Exclusion criteria
1. Severe cardiac disease2. Chronic pulmonary disease3. Significant psychiatric illness.
Outcome results
None listed