Transcutaneous Electrical Stimulation in Obstructive Sleep Apnea
Not Applicable
Completed
- Conditions
- Obstructive Sleep Apnea
- Interventions
- Device: Transcutaneous electrical stimulation
- Registration Number
- NCT04932486
- Lead Sponsor
- Sunrise
- Brief Summary
The aim of this study is to assess the efficacy of transcutaneous electrical stimulation of the upper airway muscles in patients with obstructive sleep apnea.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 42
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Transcutaneous electrical stimulation Transcutaneous electrical stimulation Participants will be asked to use the stimulator for 6 weeks at home. The study objectives will be evaluated after 6 weeks post-activation of the device.
- Primary Outcome Measures
Name Time Method Apnea-hypopnea index (AHI) 6 weeks Change from baseline to 6 weeks in the apnea-hypopnea index (AHI)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Respisom
🇧🇪Namur, Belgium