Effective Pain Management During Shoulder Replacement Surgery With EXPAREL

Withdrawn before enrolling · Phase 4

Conditions studied: Pain, Postoperative, Shoulder Osteoarthritis

In brief

The purpose of this study is to examine the effectiveness of post-operative pain control of local infiltration (LIA) of EXPAREL administration to ropivacaine administered via continuous interscalene nerve block (CINB) for postoperative pain relief following shoulder replacement. Effectiveness will be measured in opioid consumption and NRS pain intensity scores from 0-4h, 4-8h, 9-12h, 13-16h, 17-20, 21-24h, 48 hours and 72 hours post-op. Patient satisfaction with pain control; patient functional outcome; adverse events related to CINB, EXPAREL administration, and opioid consumption; and pain intensity scores from the time of surgery until post-operative day 10 (+/- 5 days) will also be examined.

Key facts

Study ID
NCT03474510
Run by
TriHealth Inc.
People needed
0
Starts
2018-03-17
Expected to finish
2019-02-01
Last updated by the study team
2021-03-01

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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