Overview
TAP Block With Liposomal Bupivacaine Versus Pre-incisional Wound Infiltration With Bupivacaine for Postoperative Pain
Status:
Terminated
Terminated
Trial end date:
2016-05-01
2016-05-01
Target enrollment:
0
0
Participant gender:
Female
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 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
University of TennesseeTreatments:
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