Superficial Cervical Plexus Blockade for Clavicle Fracture Analgesia

Withdrawn before enrolling · Phase 3 · Has a placebo group

Conditions studied: Pain, Postoperative, Satisfaction

In brief

The goal of the study is to determine if the addition of a superficial cervical plexus block to a traditional interscalene plexus block will provide superior perioperative analgesia to an interscalene brachial plexus blockade alone for repair of clavicle fractures and non-/malunions.

Key facts

Study ID

NCT03187899

Run by

University of Alabama at Birmingham

People needed

0

Starts

2018-04-01

Expected to finish

2018-12-01

Last updated by the study team

2018-05-25

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients who present for repair of isolated clavicle fractures and non-/malunions that consent to regional anesthesia and to be a part of the study.

You may not qualify if…

• Polytraumatized patients with multiple confounding injuries, patients who are not candidates for either block at the discretion of the Anesthesia Attending, patient refusal to participate in study, patient refusal of regional technique, patients with significant pulmonary disease that will not tolerate possible hemi-diaphragmatic paralysis at the discretion of the attending anesthesiologist.

Where it is running

• UAB Department of Anesthesiology and Perioperative Medicine — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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