Overview
Evaluation of Diaphragm Movement After an Interscalene Block
Status:
Recruiting
Recruiting
Trial end date:
2021-10-01
2021-10-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to evaluate the movement of the diaphragm after an interscalene block with liposome bupivacaine (LB) compared to interscalene block (IB) with bupivacaine. This study will evaluate if there is a possible prolonged phrenic nerve paralysis when using liposome bupivacaine in an interscalene block, using ultrasound.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University of Minnesota
University of Minnesota - Clinical and Translational Science InstituteTreatments:
Bupivacaine
Criteria
Inclusion Criteria:- All patients age 18 years and older who are scheduled for shoulder surgery with
interscalene block and remain in the hospital for more than 24 hours that are being
randomized into a bupivacaine versus liposomal bupivacaine interscalene block study.
Exclusion Criteria:
- Non English speaking patients.