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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02486380




Registration number
NCT02486380
Ethics application status
Date submitted
25/06/2015
Date registered
1/07/2015
Date last updated
24/06/2022

Titles & IDs
Public title
Toffee Full Face and Toffee Nasal Mask Evaluation in Obesity Hypoventilation Syndrome (NZ)
Scientific title
Toffee Full Face and Toffee Nasal Mask Evaluation in Obesity Hypoventilation Syndrome (NZ)
Secondary ID [1] 0 0
CIA-162
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Obesity Hypoventilation Syndrome 0 0
Condition category
Condition code
Respiratory 0 0 0 0
Other respiratory disorders / diseases
Diet and Nutrition 0 0 0 0
Obesity
Metabolic and Endocrine 0 0 0 0
Other metabolic disorders
Other 0 0 0 0
Research that is not of generic health relevance and not applicable to specific health categories listed above

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Devices - Toffee full face mask/toffee nasal mask

Experimental: Full face/Nasal masks - Toffee Full face/Toffee nasal


Treatment: Devices: Toffee full face mask/toffee nasal mask
Toffee full face mask/toffee nasal mask
Intervention code [1] 0 0
Treatment: Devices
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Objective Leak data
Timepoint [1] 0 0
1 night
Secondary outcome [1] 0 0
Subjective measurement of Leak
Timepoint [1] 0 0
1 night
Secondary outcome [2] 0 0
Comfort
Timepoint [2] 0 0
1 night
Secondary outcome [3] 0 0
Ease of use
Timepoint [3] 0 0
1 night
Secondary outcome [4] 0 0
Sleep efficiency
Timepoint [4] 0 0
1 night
Secondary outcome [5] 0 0
Wake after Sleep Onset (WASO)
Timepoint [5] 0 0
1 night
Secondary outcome [6] 0 0
Arousal Index (AI)
Timepoint [6] 0 0
1 night

Eligibility
Key inclusion criteria
* Aged 18+
* Diagnosed with OHS by a practicing physician
* Existing full face mask user or a nasal mask user
* Prescribed PAP therapy (Bi-Level or CPAP)
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Inability to give informed consent
* Pregnant or think they may be pregnant
* Anatomical or physiological conditions making PAP therapy inappropriate
* Patients requiring supplemental oxygen with their PAP device
* Patients who are in a coma or decreased level of consciousness
* Existing Toffee full face and Toffee nasal mask users
* No arterial PCO2 value from their medical records

Study design
Purpose of the study
Treatment
Allocation to intervention
NA
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
NA
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Stopped early
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/07/2015
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/03/2017
Sample size
Target
Accrual to date
Final
4
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
New Zealand
State/province [1] 0 0
Auckland

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Fisher and Paykel Healthcare
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Bhavi Ogra, BSc
Address 0 0
Fisher & Paykel Healthcare
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT02486380