A study evaluating the ability of a special dental device in modifying the throat width in patients with snoring and sleeping difficulties
Phase 1
Completed
- Conditions
- Health Condition 1: J988- Other specified respiratory disordersHealth Condition 2: null- Patients having obstructive sleep apnoea(OSA)
- Registration Number
- CTRI/2018/04/012923
- Lead Sponsor
- REZEEN AZIZ A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 10
Inclusion Criteria
Patients diagnosed with OSA
Patients willing for MRA therapy
Sufficient number of teeth to retain the MRA
Exclusion Criteria
Maximum mandibular protrusion of less than 6mm
Severe cariogenic status
Periodontally compromised dentition
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Increase in pharyngeal airway width after treatmentTimepoint: 1.5 Years
- Secondary Outcome Measures
Name Time Method Improvement in quality of sleep and relief from sleep apnoea and day time sleepinessTimepoint: 1.5 Years