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A clinical trial to study the effect of intraabdominal pressure guided positive end expiratory pressure on driving pressure in paediatric laparoscopic surgery

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2022/03/041242
Lead Sponsor
Rakesh Kumar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Parents willing to give consent for inclusion in study

2. Children age more than one year and less than 12 years(1-12yrs).

3. American society of anaesthesiology(ASA) physical status less than IV.

4. Elective laparoscopic surgery of more than one hour of pneumoperitoneum and in lateral position

Exclusion Criteria

1.Parental refusal to participate in the study.

2.Children with known severe lung disease.

3.Children with a history of severe lung infection having post infection sequelae in preoperative chest x-ray.

4.Children with known deformity of chest wall or thoracic spine.

5.Children with pre-existing significant cardiac, renal or hepatic diseases.

6. Children with history of previous thoracic surgery.

7.Children with BMI > 30 kg/m2

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in driving pressure in both groups at the end of pneumoperitonium.Timepoint: Change in driving pressure in the both groups at the end of pneumoperitoneum
Secondary Outcome Measures
NameTimeMethod
1.Peak airway pressure , Plateau pressure and mean airway pressure at the end of pneumoperitonium and 15 minutes interval during pneumoperitonium. <br/ ><br>2.static lung compliance at the end of pneumoperitonium and 15 minutes interval during pneumoperitonium. <br/ ><br>3.lung ultrasound score after induction and one hour after extubation. <br/ ><br>4.PaO2/FiO2 ratio, alveolar-arterial oxygen gradient and PaCO2 and ETCO2 difference <br/ ><br>5. Room air oxygen saturation <br/ ><br>6. Incidence of intraoperative hypotension and Bradycardia <br/ ><br>Timepoint: 1 at end of pneumoperitoneum <br/ ><br>2 at end of pneumoperitoneum <br/ ><br>3 after induction and 1 hour post extubation <br/ ><br>4after pneumoperitoneum and pneumoperitoneum deflation <br/ ><br>5 post-op day 1or3 or at time of discharge whichever earlier <br/ ><br>6. Intraoperative
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