NCT01944098

Intraoperative Lidocaine Infusion for Postoperative Pain Management in Obese Patients

Systemic Intraoperative Lidocaine Infusion for Postoperative Pain Management in Obese Patients: A Randomized, Placebo-Controlled Pilot Study

• Status: Completed
• Phase: Phase 3
• Study type: Interventional
• Enrollment: 20 (actual)
• Sponsor: University of South Florida · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The primary objective is to assess the feasibility and safety of administering continuous intraoperative lidocaine infusions in adult patients undergoing laparoscopic Roux en Y Gastric Bypass (RYGB). The secondary objective is to determine if lidocaine administration versus placebo (dextrose administration) (initiated at the time of anesthesia induction and continued until extubation) will reduce postoperative narcotic requirements.

Conditions

• Bariatric Surgical Pain

Interventions

Type	Name	Description
DRUG	Lidocaine
DRUG	Placebo

Timeline

• Start date: 2013-08-01
• Primary completion: 2014-07-01
• Completion: 2014-09-01
• First posted: 2013-09-17
• Last updated: 2017-10-26
• Results posted: 2017-10-26

Locations

1 site across 1 country: United States