Quadratus Lumborum Block for Abdominoplasty

Status Completed

Clinical Trial Summary

Double blinded, randomized, controlled, phase IV intervention trial. Both groups will receive a quadratus lumborum Block (QL), using ropivacaine 3.75 mg/mL in the intervention group, and sterile sodium chloride in the control group. The aim of study is to investigate the effect of a QL Block on the perioperative pain during postbariatric abdominoplasty.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02949778
Study type	Interventional
Source	Vestre Viken Hospital Trust
Contact
Status	Completed
Phase	Phase 4
Start date	November 7, 2016
Completion date	December 13, 2017

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