This study will evaluate the impact on blood glucose of the use of an oral appliance to treat obstructive sleep apnea (OSA) in individuals with Type 2 diabetes. An oral appliance is similar to a sports mouth guard or an orthodontic retainer and is an alternative treatment to continuous positive airway pressure (CPAP) for OSA. Oral appliance therapy has not been evaluated in patients with Type 2 diabetes with respect to glycemic outcomes. This will be a 1:1 randomized controlled trial: The experimental group will receive the oral appliance and the control group will receive a sham device over the course of approximately 5 months.
OSA is quite common in individuals with T2DM, occurring in as many as 60-80% of patients. The standard treatment for OSA is with the use of a CPAP machine. The CPAP provides an air pressure to keep the airways opened during sleep so that a person with OSA can breathe normally. When used appropriately, the CPAP improves sleepiness and quality of life. However, about half of the patients who receive a CPAP prescription cannot tolerate it and thus remain untreated and are potentially at increased cardiovascular and diabetes risk. In light of this, this study aims to see if the use of an alternative treatment for OSA, oral appliance therapy, where adherence is generally superior to CPAP, will improve cardiometabolic outcomes in individuals with Type 2 diabetes. This pilot trial will primarily examine feasibility and assess recruitment rates.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Fitted oral appliance
McGill University Health Centre - Research Institute
Montreal, Quebec, Canada
RECRUITINGRecruitment and retention rates
feasibility of study in T2DM
Time frame: End of study (Week 20)
Glycemic control (mean 24-hour and nocturnal glucose)
24-hour continuous glucose monitoring
Time frame: End of study (week 20)
Blood pressure
Measurement of clinic blood pressure
Time frame: End of study (Week 20)
Glucose variability
Continuous glucose monitoring system (ipro2, Medtronic)
Time frame: End of study (Week 20)
Changes in insulin or diabetes medication doses
Reporting of dose change by participant or treating physician.
Time frame: End of study (Week 20)
Systemic inflammation
hs-CRP
Time frame: End of study (Week 20)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.