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The Effects of ThermoSmartTM Technology on patient satisfaction, acceptance and compliance.

The Effects of ThermoSmartTM humidification Technology on reported satisfaction, acceptance and compliance in patients with obstructive sleep apnea, receiving continuous sportive airway pressure as their treatment.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12606000011583
Acronym
TS-BRAGa
Enrollment
32
Registered
2006-01-05
Start date
2006-03-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Participants will be randomised to receive Coninuous positive Airway Pressure (CPAP) treatment with no humidification or humidification using thermosmartTM technology. After four weeks of treatment participants will be crossed over to the alternative arm of the study. They will complete four weeks on this arm. Participants will complete a subjective questionnaire after one night and at the end of each arm of treatment (i.e. weeks four and eight) weeks. At the end of four and eight weeks objective compliance will be obtained from the CPAP device.

Interventions

Participants will be randomised to receive Coninuous positive Airway Pressure (CPAP) treatment with no humidification or humidification using thermosmartTM technology. After four weeks of treatment participants will be crossed over to the alternative arm of the study. They will complete four weeks on this arm. Participants will complete a subjective questionnaire after one night and at the end of each arm of treatment (i.e. weeks four and eight) weeks. At the end of four and eight weeks objecti

Participants will be randomised to receive Coninuous positive Airway Pressure (CPAP) treatment with no humidification or humidification using thermosmartTM technology. After four weeks of treatment participants will be crossed over to the alternative arm of the study. They will complete four weeks on this arm. Participants will complete a subjective questionnaire after one night and at the end of each arm of treatment (i.e. weeks four and eight) weeks. At the end of four and eight weeks objective compliance will be obtained from the CPAP device.

Sponsors

Fisher and Paykel Healthcare
Lead SponsorCommercial sector/Industry

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients diagnosed with OSA by 3-channel ambulatoruy system and titrated using a ful overnight PSGRDI.

Exclusion criteria

Severe cardiac diseaseChronic pulmonary diseaseSignificant psychiatric illness.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026