Overview

TAP Block With Liposomal Bupivacaine Versus Pre-incisional Wound Infiltration With Bupivacaine for Postoperative Pain

Status:
Terminated
Trial end date:
2016-05-01
Target enrollment:
0
Participant gender:
Female
Summary
In this randomized, controlled, double-blinded trial we plan to evaluate post-operative pain relief after laparoscopic-assisted Transversus Abdominis Plane (TAP) block using liposomal bupivacaine plus bupivacaine versus pre-incisional would infiltration with bupivacaine in patients undergoing Total laparoscopic or robotic assisted laparoscopic hysterectomy.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of Tennessee
Treatments:
Bupivacaine
Ketorolac
Ketorolac Tromethamine
Criteria
Inclusion Criteria:

- ASA physical status 1-3,

- Scheduled for laparoscopic or robotic assisted laparoscopic hysterectomy,

- Able to participate personally or by legal representation in informed consent

Exclusion Criteria:

- History of relevant allergy to the study drugs (Bupivacaine),

- Chronic opioid use or drug abuse history,

- Inability to understand the study protocol,

- Refusal to provide written consent,

- Soft tissue infection of the abdominal wall and skin