Comparing two methods of artificial breathing in terms of post-surgery complications during open abdominal cancer operations
Not Applicable
- Conditions
- Health Condition 1: C15-C26- Malignant neoplasms of digestive organsHealth Condition 2: C51-C58- Malignant neoplasms of female genital organsHealth Condition 3: C60-C63- Malignant neoplasms of male genital organsHealth Condition 4: C64-C68- Malignant neoplasms of urinary tract
- Registration Number
- CTRI/2019/07/020351
- Lead Sponsor
- AIIMS New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing elective open abdominal oncology surgeries
Age 18-65 years, both gender
ASA Physical Status I, II and III
Exclusion Criteria
Patients who do not give consent for the study
Patients with ASA Physical Status IV and above
Patients with Body Mass Index (BMI) < 18.5 and > 35
Patients with moderate to severe derangements in Pulmonary Function Tests
Patients with pacemakers
Surgeries in which incision does not extend above the level of umbilicus
Surgeries lasting less than two hours
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Modified Lung Ultrasound ScoreTimepoint: Before anaesthesia induction and sixty minutes after extubation
- Secondary Outcome Measures
Name Time Method HaemodynamicsTimepoint: Preoperative baseline, after induction, after intubation, after 1st recruitment, after PEEP titration, after 2nd recruitment, at start of surgery, every 30 minutes until extubation, after extubation;PaO2/FiO2 ratiosTimepoint: Before surgery, after second recruitment manoeuvre, one hour after randomization, after surgery before extubation, one hour after extubation and 24 hours after extubation;Postoperative pulmonary complicationsTimepoint: From extubation until 3 days postoperatively