A clinical trial to compare two types of ventilation during emergence in reducing post operative pulmonary complications in patients undergoing major abdominal surgeries
Not Applicable
- Conditions
- Health Condition 1: - Health Condition 2: J958- Other intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified
- Registration Number
- CTRI/2022/05/042740
- Lead Sponsor
- AIIMS New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age >18 years
ASA I to III.
Elective/Emergency major abdominal surgeries of > 2 hours duration.
Emergency abdominal surgeries which is not intubated prior to surgery.
Standardized analgesia with epidural.
Exclusion Criteria
BMI >35 kg/m2(Morbid Obesity).
Pregnancy.
Obstructive lung disease.
Underlying lung disease.
{Pneumotharx
Pulmonary tuberculosis
Pleural effusion.}.
Restrictive lung disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare Incidence of Atelectasis in pressure support group and control group during extubation and after 30 minutes of arrival to PACU.Timepoint: T1(Before induction of anaesthesia) <br/ ><br>T2(Before applying Extubation protocol) <br/ ><br>T3(After 30 mins on arrival to PACU) <br/ ><br>T4(24 hrs of Extubation)
- Secondary Outcome Measures
Name Time Method post op pulmonary complicationsTimepoint: Till third post operative day