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Clinical Trials/NCT02344615
NCT02344615
Completed
Not Applicable

A Randomized Comparison of Nerve Stimulator and Ultrasound-guided Infraclavicular Block for Upper Extremity Surgery

Cheju Halla General Hospital1 site in 1 country44 target enrollmentMay 2014
ConditionsPain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Cheju Halla General Hospital
Enrollment
44
Locations
1
Primary Endpoint
Duration of postoperative analgesia
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The investigators compared the postoperative analgesia of nerve stimulator-guided and ultrasound-guided infraclavicular block for upper extremity surgery.

Detailed Description

Ultrasound (US)-guided peripheral nerve block has increased in popularity. It has many advantages such as improved success rate, faster onset time, fewer needle passes, shorter performance time, and reduced procedural pain and vascular puncture. However, there is no information about postoperative analgesia. Therefore, the investigators tested whether ultrasound-guided peripheral nerve block enhanced the postoperative analgesia for upper extremity surgery compared with nerve stimulator (NS) guidance.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
December 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Chunwoo Yang

Department of Anesthesiology and pain medicine

Cheju Halla General Hospital

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiologists physical class I - III patients scheduled to undergo upper extremity surgery

Exclusion Criteria

  • coagulopathy, severe pulmonary disease, neuropathy, contralateral diaphragmatic paresis, allergy to study medications

Outcomes

Primary Outcomes

Duration of postoperative analgesia

Time Frame: at 24h after surgery

time from completion of local anesthetic injection until the first request for an analgesic

Secondary Outcomes

  • number of needle redirections(at 30 min after block placement)
  • patient discomfort(at 30 min after block placement)
  • paresthesia(at 30 min after block placement)
  • postoperative dysesthesia(at 24h after surgery)
  • supplemental analgesia(at 24h after surgery)
  • Pain score(at 24h after surgery)
  • Patient satisfaction(at 24h after surgery)
  • block performance time(at 30 min after block placement)
  • onset time(until 30min after completion of local anesthetic)
  • motor block of hand(at 24h after surgery)

Study Sites (1)

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