Status:

COMPLETED

Liposomal Bupivacaine vs Dexamethasone ISB

Lead Sponsor:

Hospital for Special Surgery, New York

Conditions:

Shoulder Pain

Eligibility:

All Genders

18-80 years

Phase:

PHASE4

Brief Summary

In this study, patients receiving shoulder arthroscopy will receive an interscalene block for pain management containing either liposomal bupivacaine and standard bupivacaine or standard bupivacaine a...

Eligibility Criteria

Inclusion

  • ASA I-III
  • Age 18 years or older
  • Scheduled for elective outpatient arthroscopic shoulder surgery

Exclusion

  • History of allergy to local anesthetic, or one of the study medications
  • Pre-existing neurological deficits
  • Psychiatric or cognitive disorders that prohibit patients from following study protocol
  • History of drug or alcohol abuse
  • Chronic opioid use (longer than 3 months)
  • Chronic pain syndromes
  • Infection at the site of injection
  • Patients with severe pulmonary disease
  • Herniated cervical disc, cervical myelopathy
  • Contraindication for general anesthesia and/or interscalene nerve block
  • Pregnancy
  • Open shoulder arthrotomies.
  • Non English speakers

Key Trial Info

Start Date :

July 11 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 19 2021

Estimated Enrollment :

112 Patients enrolled

Trial Details

Trial ID

NCT04047446

Start Date

July 11 2019

End Date

March 19 2021

Last Update

August 1 2022

Active Locations (1)

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Hospital for Special Surgery

New York, New York, United States, 10021