Liposomal Bupivacaine in Ambulatory Hand Surgery

Withdrawn before enrolling · Phase 3

Conditions studied: Pain

In brief

This study is being done to evaluate pain management regimens following ambulatory hand surgery. Improved pain control may be associated with decreased complications, decreased pain scores, decreased opioid dependence, improved patient comfort and satisfaction, and reduced healthcare costs. Liposomal bupivacaine is an FDA-approved local anesthetic. There will be two groups. One group will receive liposomal bupivacaine. One group will not. The results will be compared. Patients will be over the age of 18 ambulatory hand surgery. Approximately 40 subjects will participate in this study at LLU.

Key facts

Study ID
NCT02933814
Run by
Loma Linda University
People needed
0
Starts
2018-02-09
Expected to finish
2019-02-01
Last updated by the study team
2019-08-07

Who can join

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

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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