Comparison of Oxygen Delivery Devices in Post Operative Patients with Hypoxiemia: An Open Labelled Randomised Control Trial
Phase 2
- Conditions
- Health Condition 1: T885- Other complications of anesthesiaHealth Condition 2: J958- Other intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified
- Registration Number
- CTRI/2021/07/034590
- Lead Sponsor
- Aiims Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All post-op adult patients (of age 18 to 65 years) having:
•SpO2 <90% on room air.
•SpO2 <92% on nasal prongs or face mask during their PACU stay.
Exclusion Criteria
-Patients with abnormalities of face or who are post-surgery of face, nose or airway
-Patients Post Thoracotomy and Lung surgeries
-Patients with pre-existing pulmonary complications
-Patients who underwent Head and Neck surgery
-Patients having episodes of Vomiting or Haemoptysis
•Patients underwent upper Gastro-intestinal surgery
•Pregnant women
•SPO2 >92%
•Intubated patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in P/F ratio after 2 hours of use of oxygen delivery devices in Post Anaesthesia Care UnitTimepoint: 2 hours
- Secondary Outcome Measures
Name Time Method Change in blood gas levels (PaO2, PaCO2) <br/ ><br>Patient comfort and ease of communicationTimepoint: Two hours