A study to check the effects of the mask breathing device on the wellness of sleep in patients who are seriously ill and admitted to the critical care unit of hospital.
Not Applicable
- Conditions
- Health Condition 1: J962- Acute and chronic respiratory failure
- Registration Number
- CTRI/2023/06/054124
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Age >18 years
2. All voluntary, oriented participants in ICU
3. Patients receiving NIV as a primary mode of
treatment
4. Overnight NIV support.
Exclusion Criteria
1. Intermittent NIV treatment and oxygen therapy.
2. Palliative care.
3. Post-extubation NIV treatment.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of sleep among non-invasively ventilated patientsTimepoint: Participants will be assessed daily after 24 hours of NIIV initiation until they are either intubated or weaned from NIV.
- Secondary Outcome Measures
Name Time Method Factors affecting the quality of sleep in CCU & effects of quality of sleep on weaning off from NIV. <br/ ><br>Timepoint: Participants will be assessed daily after 24 hours of NIIV initiation until they are either intubated or weaned from NIV.