Comparing Liposomal Bupivacaine Versus Standard Bupivacaine in Colorectal Surgery

Completed · Phase 3

Conditions studied: Colorectal Surgery

In brief

The purpose of this study is to compare the difference between two different pain control methods in patients who will be having a colorectal surgery

Key facts

Study ID

NCT03702621

Run by

Indiana University

People needed

90

Starts

2018-08-30

Expected to finish

2020-03-13

Last updated by the study team

2023-05-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients undergoing colorectal surgery at Indiana University Hospital
• American Society of Anesthesiologists (ASA) class 1, 2, 3 or 4
• Age 18 or older, male or female
• Desires Regional anesthesia for postoperative pain control

You may not qualify if…

• Any contraindication for QL block.
• History of substance abuse in the past 6 months.
• Patients on more than 30mg morphine equivalents of opioids daily.
• Any physical, mental or medical conditions which in the opinion of the investigators, may confound quantifying postoperative pain resulting from surgery.
• Known allergy or other contraindications to the study medications (Acetaminophen, Gabapentin, Bupivacaine).
• Postoperative intubation.
• Any BMI greater than 40.0.

Where it is running

• Indiana University Hospital — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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