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Comparison of two modes of artificial respiration during anaesthesia for emergency operation of belly

Not Applicable
Conditions
Health Condition 1: K929- Disease of digestive system, unspecified
Registration Number
CTRI/2020/12/029765
Lead Sponsor
Dr Emmanuel Easterson E
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Adult patients (aged between 18 years and 75 years), of either sex undergoing Emergency Laparotomy for non-traumatic indications (of an expected duration of more than 2h) under general anaesthesia will be recruited in this study

Exclusion Criteria

Exclusion criteria

1.Patients refusal to participate in the study

2.Patients undergoing emergency laparotomy for trauma and related causes.

3.Known COPD or other chronic lung diseases

4.Preoperative diagnosis of Pneumonia

5.Known deformity of chest wall or thoracic spine

6.Pre-existing significant cardiac, renal and hepatic diseases

7.Patients with history of previous thoracic surgery.

8.BMI > 30 kg/m2, < 18 kg/m2

9.Patients who are on high dose of vasopressors (defined as noradrenalin 10mcg/m or equivalent)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postoperative pulmonary complicationsTimepoint: Till postoperative day 7
Secondary Outcome Measures
NameTimeMethod
1. Duration of hospital stay <br/ ><br>2. Duration of ICU stay <br/ ><br>3. Hospital mortalityTimepoint: Till hospital discharge;1. Oxygenation status <br/ ><br>2. Incidence of hypotension and bradycardia <br/ ><br>3. Requirement of rescue therapy <br/ ><br>Timepoint: Intraoperative period;Oxygen free daysTimepoint: Till day 28 of randomization
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