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Efficacy of Liposomal Bupivacaine Versus 0.25% Bupivacaine for Laparoscopic Urologic Surgery

Phase 4
Completed
Conditions
Pain, Postoperative
Interventions
Registration Number
NCT02222129
Lead Sponsor
Knight, Richard, M.D.
Brief Summary

A prospective, randomized comparison of bupivacaine to liposomal bupivacaine given by local injection at all the wound sites in patients undergoing robotic-assisted or laparoscopic urologic surgeries in an effort to determine which method reduced postoperative opioid use the most.

Detailed Description

Liposomal bupivacaine was developed to extend the duration of efficacy of bupivacaine from the typical 6 - 8 hours up to 72 hours. The prolonged duration of liposomal bupivacaine was initially demonstrated in mice in 1994. Two randomized controlled trials using liposomal bupivacaine for bunionectomy and hemorrhoidectomy resulted in FDA approval for its use in humans. More recently, liposomal bupivacaine has also been found to improve pain control for patients undergoing total knee arthroplasty. Infiltration of a local anesthetic into laparoscopic port sites is a common practice that has been shown in some studies to improve postoperative pain. To compare liposomal bupivacaine and 0.25% bupivacaine for local analgesia following laparoscopic and robotic urologic surgery, a randomized comparison-controlled trial was performed.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
206
Inclusion Criteria
  • At least 18-years-old, undergoing laparoscopic urologic surgery.
Exclusion Criteria
  • Pregnant and/or nursing mothers.
  • Allergy to bupivacaine.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Liposomal bupivacaineliposomal bupivacaineSurgical site infiltration of liposomal bupivacaine.
BupivacaineBupivacaineSurgical site infiltration of 0.25% bupivacaine.
Primary Outcome Measures
NameTimeMethod
Total Opioid Consumption Measured in Intravenous Morphine Equivalents During the Postoperative Hospital StayAll data was recorded during the patient's hospital stay, typically less than 5 days. All data was tabulated from the electronic medical record, typically within 30 days of discharge from hospital.

Total opioid consumption measured in intravenous morphine equivalents during the postoperative hospital stay

Secondary Outcome Measures
NameTimeMethod
Visual Analog Pain Scores.All data was recorded during the patient's hospital stay, typically less than 5 days. All data was tabulated from the electronic medical record, typically within 30 days of discharge from hospital.

Visual analog pain scores.

Length of Hospital Stay.All data was recorded during the patient's hospital stay, typically less than 5 days. All data was tabulated from the electronic medical record, typically within 30 days of discharge from hospital.

Length of hospital stay.

Time to First Opioid Use.All data was recorded during the patient's hospital stay, typically less than 5 days. All data was tabulated from the electronic medical record, typically within 30 days of discharge from hospital.

Time to first opioid use.

Trial Locations

Locations (2)

Baptist Health System

🇺🇸

San Antonio, Texas, United States

Methodist Healthcare System

🇺🇸

San Antonio, Texas, United States

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