drugset / Trial / NCT02154763

The Use of Intraperitoneal Ropivacaine in Bariatric Bypass Surgery

NCT02154763

Phase 3 Completed 120 enrolled Ottawa Hospital Research Institute
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a pilot study in a randomized, controlled, double-blinded format and will evaluate the ability of a local anesthetic, Ropivacaine, to decrease pain after gastric bypass surgery. The drug will be administered into the abdomen during a bariatric bypass surgery. After surgery, patients who received Ropivacaine will be compared to those without Ropivacaine to determine its effect on reducing pain, recovery of lung function, ability to walk, and quality of life during recovery.

Timeline

Start
2014-07
Primary completion
2015-01
Completion
2015-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropivacaine Other / unclassified 200 mg Other

Indications

No indication recorded.