Comparison of two devices oxygen therapy for the management of low oxygen respiratory failure in post operative patients.
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/05/042630
- Lead Sponsor
- Department of anesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Study population 18-60 years age group
ASA grade 1;2
Surgical duration more than 2 hrs
PaO2 <60 mmHg
Exclusion Criteria
Post operative patients who did not recieve HFNC after extubation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of patients requiring reintubationTimepoint: 48 hrs
- Secondary Outcome Measures
Name Time Method Rate of escalation of respiratory support and pulmonary complication in post operative adult surgical patientsTimepoint: 1 month
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie high-flow nasal oxygen therapy in acute hypoxemic respiratory failure?
How does high-flow nasal oxygen plus noninvasive ventilation compare to standard oxygen therapy in post-operative hypoxemic patients?
Which biomarkers predict response to noninvasive ventilation in post-surgical acute respiratory failure?
What adverse events are associated with combined high-flow nasal oxygen and noninvasive ventilation in post-op care?
Are there alternative oxygen delivery systems to high-flow nasal therapy for managing post-operative hypoxemia?