Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12616000740493
Ethics application status
Approved
Date submitted
31/05/2016
Date registered
6/06/2016
Date last updated
12/07/2018
Type of registration
Prospectively registered

Titles & IDs
Public title
Oral appliance with built in airway for the treatment of obstructive sleep apnoea.
Scientific title
Safety and efficacy of Oventus O2Vent and the effect of incorporation of an enclosed airway on compliance in patients with obstructive sleep apnoea
Secondary ID [1] 289313 0
OVEN-003
Secondary ID [2] 289346 0
nil known
Universal Trial Number (UTN)
U1111-1183-2961
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
obstructive sleep apnoea 298913 0
Condition category
Condition code
Respiratory 298985 298985 0 0
Sleep apnoea

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
The Oventus O2Vent is an oral appliance similar in appearance to a mouth guard. It is a modification to the Oventus Clearway, designed to treat snoring and sleep apnoea. It is made up of two parts. The main structure which forms the breathing port at the front leading to the airways on each side to the rear of the appliance, is made from polished medical grade titanium with a polymer insert. The lower portion is made from dual laminate and is positioned in an advanced position to bring the jaw forward. Further adjustment of the jaw position is much easier with a screw mechanism.

The device will be delivered by a dentist in a dedicated dental clinic. Eligibility for a dental appliance will have been confirmed on a visit prior to enrollment into the trial. The appliance is custom made and has a built in airway to allow airflow through the device. The device will be fitted by the dentist with either the built in airway open (Treatment 1) or closed (Treatment 2). During the dental fitting, the dentist will check the fit of the appliance and provide instructions on use and cleaning. The device will be worn every night during sleep and removed on waking for the duration of the study. During an acclimatization phase of 2-8 weeks, ongoing symptoms, side effects, comfort and usage will be assessed via questionnaires every 2 weeks and device adjusted to achieve optimal lower jaw advancement. When treatment has been optimized, efficacy may be confirmed using a level 3 home sleep study to inform clinical opinion that treatment is optimized. Comfort and compliance will then be assessed using a questionnaire and sleep diary over a 2 week period with efficacy established on a level 1 in laboratory sleep study at the end of the 2 weeks.. Participants will then cross over into the other Treatment group and comfort, compliance and efficacy assessed over a 2 week period as described.. In the interest of not withdrawing treatment, there is no washout period between the 2 treatment arms.
Intervention code [1] 294867 0
Treatment: Devices
Comparator / control treatment
Comfort and compliance with the airway open (Treatment 1) will be compared to comfort and compliance with the airway closed (Treatment 2). Airway closed will be considered as the control.
Control group
Active

Outcomes
Primary outcome [1] 298482 0
Difference in compliance with airway open and closed assessed using a 2 week participant self-reported sleep diary.
Timepoint [1] 298482 0
Compliance assessed for a period of 2 weeks on each treatment arm, following a 2-8 week period of acclimatization and optimization of jaw position.

Primary outcome [2] 298483 0
Device related adverse events.
Known device related events include the following assessed via questionnaires:
1. Excess salivation
2. Dry mouth
3. Gum irritation
4. Cheek or tongue pain
5. Jaw discomfort/pain
6. Jaw set (lock)
7. Tooth movement or loosening
8. Tooth discomfort/pain

The questionnaire used to assess side effects is part of the Usage and Comfort questionnaire developed internally for the study to enable clinicians to evaluate and monitor side effects and acclimatization to treatment.
Timepoint [2] 298483 0
Compliance assessed at over 2 weeks on active Treatment 1 and Treatment 2 with data collected and entered into the EDC at the end of the 2 week period.
Adverse events assessed during acclimatization phase every 2 weeks and after 2 weeks on each treatment.
Primary outcome [3] 298484 0
Change in Apnoea-Hypopnoea Index (AHI) from baseline to treatment with O2Vent airway open.
Timepoint [3] 298484 0
AHI assessed at baseline using polysomnography and again at the end of 2 weeks on active treatment (Treatment 1), following a period of acclimatization and optimization of jaw position.
Secondary outcome [1] 324293 0
Response rate in subjects with nasal congestion using rhinomanometry as an objective measure of nasal congestion. Response rate is defined as a greater than or equal to 50% reduction in AHI.
Timepoint [1] 324293 0
Nasal congestion assessed prior to polysomnography on the last night of active treatment. Response rate is calculated from the polysomnogrphy defined AHI.

Eligibility
Key inclusion criteria
1. Age greater than or equal to 18 years old.
2. Obstructive sleep apnoea as diagnosed by a sleep physician within the last 12 months (diagnoses from polysomnography) and:
a) Recommended for oral appliance therapy as at least part of the treatment or
b) Recommended CPAP but are CPAP Intolerant as documented by affidavit.
3. Eligible to receive a mandibular advancement device
4. Must have at least 8 upper and 8 lower teeth
5. Is able to provide written informed consent to all study procedures and agrees to adhere to all protocol requirements.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Pregnant or lactating females
2. Participating in another clinical trial
3. Periodontal disease
4. Exaggerated gag reflex
5. Medication usage that could influence respiration or sleep (e.g. regular use of sedatives, heavy alcohol consumption)
6. OSA with uncontrolled or untreated cardiovascular disease
7. Central Sleep Apnoea events (greater than or equal to 5/hr)
8. Previous Uvulopalatopharyngoplasty (UPPP)
9. Severe somatic or psychiatric disorders
10. Periodic limb disorder
11. Reversible morphological upper airway abnormalities e.g. enlarged tonsils
12. Temporomandibular disorders
13. Dental pain

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation via sealed envelopes.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomization in permuted blocks will be performed to achieve balance across treatment groups.
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



The people analysing the results/data
Intervention assignment
Crossover
Other design features
sleep studies analysed with scorer blinded to treatment.
Phase
Not Applicable
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis
Compliance (Nightly Usage): Prior data indicate that nightly use of the first generation Oventus appliance was average 7 hours with SD of 2. For a 10% reduction in usage with airway closed, we expect a difference of 0.7, and using SD of differences of 1, we will need to study 29 subjects to be able to reject the null hypothesis that this response difference is zero with probability (power) 0.95. The Type I error probability associated with this test of this null hypothesis is 0.05. Paired t tests will be used to compare Treatment 1 and Treatment 2 compliance.

A total of 40 subjects will be recruited to allow for 25% drop out rate.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
18/07/2016
Actual
25/07/2016
Date of last participant enrolment
Anticipated
31/12/2016
Actual
9/03/2017
Date of last data collection
Anticipated
31/08/2017
Actual
15/05/2018
Sample size
Target
40
Accrual to date
Final
43
Recruitment in Australia
Recruitment state(s)
QLD
Recruitment hospital [1] 5878 0
Breathing Assist Solutions - Indooroopilly
Recruitment postcode(s) [1] 13323 0
4068 - Indooroopilly

Funding & Sponsors
Funding source category [1] 293711 0
Commercial sector/Industry
Name [1] 293711 0
Oventus Pty Ltd
Country [1] 293711 0
Australia
Primary sponsor type
Commercial sector/Industry
Name
Oventus Pty Ltd
Address
1 Swann Road
Indooroopilly QLD 4068
Country
Australia
Secondary sponsor category [1] 292545 0
None
Name [1] 292545 0
Address [1] 292545 0
Country [1] 292545 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 295146 0
Bellberry Limited
Ethics committee address [1] 295146 0
Ethics committee country [1] 295146 0
Australia
Date submitted for ethics approval [1] 295146 0
06/06/2016
Approval date [1] 295146 0
29/06/2016
Ethics approval number [1] 295146 0

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

Contacts
Principal investigator
Name 66218 0
Dr Damian Lavery
Address 66218 0
Breathing Assist Solutions
1 Swann Road
Indooroopilly QLD 4068
Country 66218 0
Australia
Phone 66218 0
+61 7 3180 3193
Fax 66218 0
Email 66218 0
[email protected]
Contact person for public queries
Name 66219 0
Irene Szollosi
Address 66219 0
Oventus Pty Ltd
1 Swann Road
Indooroopilly QLD 4068
Country 66219 0
Australia
Phone 66219 0
+61 1300 533 159
Fax 66219 0
Email 66219 0
[email protected]
Contact person for scientific queries
Name 66220 0
Chris Hart
Address 66220 0
Oventus Pty Ltd
1 Swann Road
Indooroopilly QLD 4068
Country 66220 0
Australia
Phone 66220 0
+61 1300 533 159
Fax 66220 0
Email 66220 0
[email protected]

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

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.