Analgesic Efficacy of Liposomal Bupivacaine vs. Bupivacaine HCL as a Tap Block After Abdominally Based Autologous Breast Reconstruction



Status:Terminated
Healthy:No
Age Range:18 - Any
Updated:2/20/2019
Start Date:February 29, 2016
End Date:March 8, 2018

Use our guide to learn which trials are right for you!

A Prospective Trial to Assess Analgesic Efficacy of Liposomal Bupivacaine vs. Bupivacaine HCL as a Tap Block After Abdominally Based Autologous Breast Reconstruction

This study will evaluate the efficacy of analgesia provided by liposomal bupivacaine
(Exparel) when compared to bupivacaine HCL as a transverse abdominis plane (TAP) block in
terms of discharge milestones, opioid use, costs, and patient-reported satisfaction at 12,
24, and 72 hours. The investigators propose that Exparel will lower opioid use, length of
stay, and overall cost of abdominally-based autologous breast reconstruction, and will lead
to greater patient satisfaction.


Inclusion Criteria:

- Scheduled for abdominal-based autologous breast reconstruction (DIEP, MS-TRAM, or
TRAM).

- At least 18 years of age.

- Female.

- Able to understand and willing to sign a written informed consent document.

Exclusion Criteria:

- Cognitive impairment.

- History of abdominal surgery precluding free flap donor site.

- Allergy or intolerance to bupivacaine or "amide" anesthetics.

- Significant preoperative chronic pain (requiring daily narcotics) or neuropathic pain
(requiring daily use of pregabalin or gabapentin) within the previous 3 months.

- Pregnant or breastfeeding.
We found this trial at
1
site
660 S Euclid Ave
Saint Louis, Missouri 63110
(314) 362-5000
Principal Investigator: Terence Myckatyn, M.D.
Phone: 314-996-8800
Washington University School of Medicine Washington University Physicians is the clinical practice of the School...
?
mi
from
Saint Louis, MO
Click here to add this to my saved trials