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Clinical Trials/NCT05020821
NCT05020821
Completed
Not Applicable

Superior Trunk Block Catheter Versus Single-shot Superior Trunk Block With Intravenous Dexmedetomidine for Shoulder Arthroplasty

Yonsei University1 site in 1 country92 target enrollmentSeptember 2, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Shoulder Arthroplasty
Sponsor
Yonsei University
Enrollment
92
Locations
1
Primary Endpoint
Numeric rating scale pain score
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Shoulder arthroplasty is associated with significant postoperative pain. Appropriate pain control after shoulder arthroplasty is crucial for postoperative rehabilitation and patient satisfaction. Superior trunk block is a commonly employed regional anesthetic technique for shouler arthroplasty, and a continuous catheter is often placed to extend the analgesic benefit of the block. However, continuous peripheral nervel block (PNB) is more costly and time-consuming than sigle-shot PNB. Recent evidence suggests that intravenous (IV) dexmedetomidine (DEX) prolong the analgesic duration after sigle-shot PNB. The investigators will compare continuous superior trunk block with single-shot superior trunk block with IV DEX in patients undergoing shoulder arthroplasty.

Registry
clinicaltrials.gov
Start Date
September 2, 2021
End Date
August 10, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 1 Patients aged 19 years old or older, with American Society of Anesthesiologists Physical Status 1-3, and scheduled for elective shoulder arthroplasty

Exclusion Criteria

  • Allergy or intolerance to any of the drugs used in the study
  • Heart failure
  • Hepatic or renal insufficiency
  • Opioid dependency
  • Coagulopathy
  • Pre-existing neurologic or anatomic deficits in the upper extremities
  • Severe psychiatric illness

Outcomes

Primary Outcomes

Numeric rating scale pain score

Time Frame: 24 hours after the end of surgery

Pain intensity at rest will be evaluated by an 11-point numeric rating scale (NRS: 0 = no pain, 10 = worst imaginable pain) 24 hours after the surgery.

Study Sites (1)

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