Transverse Abdominis Plane Block in Laparoscopic Ventral Hernia Repair

Status Completed

Clinical Trial Summary

The current study aims to determine if transverse abdominis plane block using local anesthetic agents (bupivacaine 0.25% + Ropivacaine 0.20%) decreases the post operative pain and helps in early mobilization or discharge from hospital in patients undergoing laparoscopic ventral hernia repair.

Clinical Trial Description

Patients meeting inclusion criteria would be randomised after admission. Those patients in experimental arm shall receive the TAP block under USG guidance while those in control arm do not receive any block. Surgery shall be proceeded in the usual manner in all the patients and assessment for pain starts in the immediate post operative or recovery room after the patient is completely conscious. The total amount of analgesic required by the patient is measured. Pain assessment is done using the visual analog scale (VAS) at regular intervals until follow up review. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03342040
Study type	Interventional
Source	GEM Hospital & Research Center
Contact
Status	Completed
Phase	N/A
Start date	October 15, 2017
Completion date	February 1, 2019

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