drugset / Trial / NCT02949778

Quadratus Lumborum Block for Abdominoplasty

NCT02949778 ↗

Phase 4 Completed 50 enrolled Vestre Viken Hospital Trust
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2016-11-07
Primary completion
2017-06-15
Completion
2017-12-13

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ropivacaine Other / unclassified 3.75 mg/ml —

Indications