Intraperitoneal instillation of local anaesthetic (IPILA) in laparoscopic bariatric surgery

Phase 4

Completed

• Conditions: Bariatric surgery; Post-operative pain; Obesity; Anaesthesiology - Pain management; Surgery - Surgical techniques; Diet and Nutrition - Obesity

• Registration Number: ACTRN12618000389202
• Lead Sponsor: Dr Nicholas Williams

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-03-15
• Study Completion: 2020-11-30
• Last Update Posted: 5 July 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 105

Inclusion Criteria

Patients who are undergoing a laparoscopic bariatric procedure through Riverina Bariatrics

Exclusion Criteria

allergy to local anaesthetic, severe cardiovascular disease (congestive heart failure or ischaemic heart disease), chronic renal disease (creatinine clearance <60 mL/h), child-Pugh Score B/C and if the participant declined to participate.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Post-operative pain assessed using the 100mm visual analogue scale [Post-operatively in recovery at 1 & 2 hours and at 4, 8, 24, 48 hours. ]

Secondary Outcome Measures

Name	Time	Method
Morphine consumption or morphine equivalents post-operatively in mg/kg which will be assessed by examining post-operative medication charts and patient records. [In recovery at 2 hours and at 24 and 48 hours post-operatively.];Length of stay post-operatively which will be assessed by examining patient's hospital records. [Measured at time of discharge]