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Clinical Trial Summary

This study investigated the effectiveness of a surgeon administered, laparoscopic guided, regional anaesthesia technique.


Clinical Trial Description

A prospective, double blind, randomised controlled trial was performed. Consenting patients undergoing laparoscopic cholecystectomy were randomised, by envelope, to a laparoscopic guided 2-point blockade (subcostal transversus abdominis plane and rectus sheath) using either Chirocaine® 2.5mg/ml (LaGRA) or 0.9% Saline (Placebo) after specimen extraction.

Primary endpoints were post-operative pain in the first 6 hours. Secondary endpoints were analgesic/anti-emetic usage and day case and re-admission rates. Data was analysed using GraphPad Prism (V7). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03394807
Study type Interventional
Source Health Service Executive, Ireland
Contact
Status Completed
Phase Phase 4
Start date October 1, 2016
Completion date August 30, 2017

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