Clinical trial to study the convenience and usability of newly proposed adaptive positive airway pressure mask for obstructive sleep apnea
Not Applicable
- Conditions
- Health Condition 1: J962- Acute and chronic respiratory failure
- Registration Number
- CTRI/2024/04/066167
- Lead Sponsor
- Department of Science and Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Subjects with AHI greater than 5
Subjects complaining of hypersomnia
Mild and moderate sleep apnea
subjects with increased carbon dioxide level
Exclusion Criteria
Severe or chronic respiratory ailment
Subjects diagnosed with pneumothorax
Subjects with Hypercapnia, Respiratory acidosis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method reduction in AHI (Apnea Hypopnea Index) of the user, SpO2 will be improved during therapyTimepoint: min 4 to 8 hours of single time usage during night sleep
- Secondary Outcome Measures
Name Time Method improved sleep cycle, reduced ODI (oxygen desaturation index), SQI (sleep quality index) will be improved.Timepoint: from 2 weeks of usage.