Impact of Interface With/Without Oral Appliance of Sleep Apnea Treatment
Primary Purpose
Obstructive Sleep Apnea
Status
Terminated
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Nasal mask and oral appliance vs oro-nasal mask during autoCPAP therapy
Sponsored by
About this trial
This is an interventional treatment trial for Obstructive Sleep Apnea focused on measuring CPAP compliance, leaks, Respiratory disturbances index, quality of life
Eligibility Criteria
Inclusion Criteria:
- normal nasal breathing
- dentition allowing for use of an oral appliance
- absence of mandibular joint pathology
- Patients requiring the use of a facial mask during CAPP titration due to presence of mouth leaks with a nasal/prong interface
- Patients using CPAP less than 3 hours/day as prescribed following CPAP titration
Exclusion Criteria:
- Clinical instability
- smoking cessation
- current weight loss strategy
- Marked anatomic abnormalities of upper airway (i.e. macroglossia, tonsils hypertrophy)
- severe cardio-metabolic co-morbidity
Sites / Locations
- CHUM
- IUCPQ
- AGIRADOM
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
oro-nasal mask
Nasal mask and oral appliance
Arm Description
Oro-nasal mask during 1 month of auto CPAP
Nasal mask and oral appliance during 1 month of auto CPAP
Outcomes
Primary Outcome Measures
CPAP compliance
CPAP compliance will be assessed according to machine report download for the 4 weeks of treatment in each study condition.
Secondary Outcome Measures
diurnal somnolence
Epworth Sleepiness Score
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01889472
Brief Title
Impact of Interface With/Without Oral Appliance of Sleep Apnea Treatment
Official Title
Impact of Nasal Mask/Oronasal Mask on Compliance to Treatment With Continuous Positive Airway Pressure (CPAP) in Patients With Obstructive Sleep Apnea
Study Type
Interventional
2. Study Status
Record Verification Date
May 2017
Overall Recruitment Status
Terminated
Why Stopped
Inability to further include additional patients
Study Start Date
June 2013 (undefined)
Primary Completion Date
January 18, 2017 (Actual)
Study Completion Date
January 18, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Laval University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
CPAP is the most effective treatment of obstructive sleep apnea. Oro-nasal masks may be used in case of mouth leaks but these are associated with higher positive pressure needs and lower compliance to treatment. The present investigation evaluates if CPAP compliance would increase when an oral appliance is used in combination with a nasal mask compared to the use of an oro-nasal mask. Eligible patients are those demonstrating a low compliance when using an oro-nasal mask during CPAP therapy. Patients will be treated with automatic CPAP with one of the above-detailed interfaces for 4 weeks and data will be extracted from the machine report in each condition.
Detailed Description
Participating subjects will be currently treated by CPAP and low compliance will be assessed according to machine report download demonstrating 3h or less of CPAP usage per night.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea
Keywords
CPAP compliance, leaks, Respiratory disturbances index, quality of life
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
oro-nasal mask
Arm Type
Active Comparator
Arm Description
Oro-nasal mask during 1 month of auto CPAP
Arm Title
Nasal mask and oral appliance
Arm Type
Experimental
Arm Description
Nasal mask and oral appliance during 1 month of auto CPAP
Intervention Type
Device
Intervention Name(s)
Nasal mask and oral appliance vs oro-nasal mask during autoCPAP therapy
Primary Outcome Measure Information:
Title
CPAP compliance
Description
CPAP compliance will be assessed according to machine report download for the 4 weeks of treatment in each study condition.
Time Frame
After 4 weeks of CPAP trial
Secondary Outcome Measure Information:
Title
diurnal somnolence
Description
Epworth Sleepiness Score
Time Frame
After 4 weeks of CPAP trial
Other Pre-specified Outcome Measures:
Title
Respiratory disturbances index
Description
Provided by CPAP report
Time Frame
After 4 weeks of CPAP trial
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
normal nasal breathing
dentition allowing for use of an oral appliance
absence of mandibular joint pathology
Patients requiring the use of a facial mask during CAPP titration due to presence of mouth leaks with a nasal/prong interface
Patients using CPAP less than 3 hours/day as prescribed following CPAP titration
Exclusion Criteria:
Clinical instability
smoking cessation
current weight loss strategy
Marked anatomic abnormalities of upper airway (i.e. macroglossia, tonsils hypertrophy)
severe cardio-metabolic co-morbidity
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frederic Series, MD
Organizational Affiliation
Fondation IUCPQ
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHUM
City
Montreal
State/Province
Quebec
Country
Canada
Facility Name
IUCPQ
City
Quebec
ZIP/Postal Code
G1V 4G5
Country
Canada
Facility Name
AGIRADOM
City
Grenoble
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
23691209
Citation
Borel JC, Tamisier R, Dias-Domingos S, Sapene M, Martin F, Stach B, Grillet Y, Muir JF, Levy P, Series F, Pepin JL; Scientific Council of The Sleep Registry of the French Federation of Pneumology (OSFP). Type of mask may impact on continuous positive airway pressure adherence in apneic patients. PLoS One. 2013 May 15;8(5):e64382. doi: 10.1371/journal.pone.0064382. Print 2013.
Results Reference
background
PubMed Identifier
30689098
Citation
Leotard A, Lesgoirres M, Daabek N, Lebret M, Bailly S, Verain A, Series F, Pepin JL, Borel JC. Adherence to CPAP with a nasal mask combined with mandibular advancement device versus an oronasal mask: a randomized crossover trial. Sleep Breath. 2019 Sep;23(3):885-888. doi: 10.1007/s11325-018-01772-5. Epub 2019 Jan 28.
Results Reference
derived
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Impact of Interface With/Without Oral Appliance of Sleep Apnea Treatment
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