Study to test a method of detecting lung complications after laparoscopic surgeries
- Conditions
- Health Condition 1: 4- Measurement and Monitoring
- Registration Number
- CTRI/2021/11/038118
- Lead Sponsor
- Intramural funding JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1) Patients between 18 and 75 years of age planned for laparoscopic abdominal surgeries under general
anesthesia in Trendelenburg position
2) Duration of surgery more than 2 hours (from the time of creation of the pneumoperitoneum) like surgeries for prostate, rectum, total laparoscopic hysterectomy, etc.
3) Patients expected to be extubated on table post
operatively
1) Patients with history of acute respiratory distress syndrome
2) Pregnant patients
3) Patients with cardiac comorbidities of NYHA class III and IV
4) Patients with valvular heart diseases
5) Patients with history of stroke
6) Patients with elevated intracranial pressure
7) Previous lung surgery
8) Severe Chronic obstructive pulmonary disease
(COPD) with Forced expiratory volume/Forced vital
capacity (FEV1/FVC) <60%
9) History of progressive neuromuscular illness
10) Refusal to participate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare modified Lung Ultrasound Score (LUSS) in <br/ ><br>patients undergoing laparoscopic abdominal surgeries under general anesthesia with targeted driving pressures and <br/ ><br>conventional ventilation strategiesTimepoint: Baseline (preoperative), <br/ ><br>15 to 30 minutes after extubation <br/ ><br>
- Secondary Outcome Measures
Name Time Method