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Clinical Trials/NCT02014766
NCT02014766
Unknown
Not Applicable

A Randomized Comparison of Ultrasound-guided Supraclavicular and Interscalene Block After Shoulder Surgery

Cheju Halla General Hospital1 site in 1 country50 target enrollmentNovember 2013
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ConditionsPain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Cheju Halla General Hospital
Enrollment
50
Locations
1
Primary Endpoint
pain duration
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

We hypothesize that both ultrasound-guided supraclavicular and interscalene block provide similar analgesia after shoulder surgery.

Detailed Description

Interscalene block provides effective postoperative analgesia after shoulder surgery. However, it can be associated with significant risk including the phrenic nerve palsy. Previous study reported that ultrasound-guided interscalene and supraclavicular blocks are effective and safe for shoulder arthroscopy.

Registry
clinicaltrials.gov
Start Date
November 2013
End Date
December 2014
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •American Society of Anesthesiologists physical status I-III inpatients undergoing shoulder surgery

Exclusion Criteria

  • •pregnancy, severe respiratory disease, preexisting neuropathy in the operated arm, coagulopathy, allergy to study medication

Outcomes

Primary Outcomes

pain duration

Time Frame: at 24h after operation

Secondary Outcomes

  • diaphragmatic movement(preoperative, after block(at 30 min), after operation)
  • motor block(after block(at 30 min), after operation, at 24h)
  • paresthesia(after block(at 30min), after operation, at 24h)
  • complications(after block (at 30 min), after operation, at 24h)
  • supplemental analgesia(after operation, at 24h)
  • pain score(at 24h)
  • patient satisfaction(at 24h)

Study Sites (1)

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