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Study identifier: NCT05824832 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Buprenorphine, Clonidine, and Dexamethasone on Duration of Brachial Plexus Blocks for Upper Extremity Surgery

Condition: Pain, Postoperative  ·  Sponsor: Loyola University

PhasePhase 4
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn if there is a difference in morphine requirements in patients after upper extremity surgeries including shoulder arthroscopy. The main question it aims to answer is whether there is a difference between Interscalene brachial plexus blocks with the addition of buprenorphine, dexamethasone, and clonidine and the same block without the adjuvant.

This description comes directly from the study's public registry record.

Talk to the study team

Susan Fargo  ·  708-216-8046  ·  sfargo@luc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Loyola University ChicagoMaywood, Illinois, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05824832