Testing Lung functions before major Surgical operations
Not Applicable
- Registration Number
- CTRI/2023/06/053950
- Lead Sponsor
- VIJAYANAGAR INSTITUTE OF MEDICAL SCIENCES
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients posted for Elective upper abdominal and thoracic surgeries (excluding cardiac) under general anaesthesia with / without regional anaesthesia
Age group 20 to 70 yrs, of either sex
American Society of Anesthesiologists (ASA) physical status I-III
Exclusion Criteria
Patient refusal
Patients not likely / not able to comprehend and follow the instructions on spirometry use
Patients with limited mouth opening / painful / infective oral conditions
Patients with polytrauma
Pregnant patients
Surgeries under local anaesthesia and outpatient surgeries
Patients with significant cardiac, neurological and other systemic disorders
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of adverse respiratory events revealed by spirometry in post anaesthesia care unitTimepoint: from before surgery to two hours after surgery
- Secondary Outcome Measures
Name Time Method Changes in spirometric parameters (FVC, FEV1/FVC, PEFR, MMFR, MBC, FV loops, etc) patient wiseTimepoint: from before surgery to two hours after surgery