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Clinical Trials/NCT04101266
NCT04101266
Completed
Not Applicable

Comparison of the Effects Combined Suprascapular and Infraclavicular Nerve Blocks to Interscalene Nerve Block Applied Arthtroscopic Shoulder Surgery

Diskapi Yildirim Beyazit Education and Research Hospital1 site in 1 country76 target enrollmentSeptember 30, 2019
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ConditionsArthroscopic Shoulder Surgery

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Arthroscopic Shoulder Surgery
Sponsor
Diskapi Yildirim Beyazit Education and Research Hospital
Enrollment
76
Locations
1
Primary Endpoint
postoperative pain: numeric rating scale (NRS)
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

It is compared that combined suprascapular and infraclavicular nerve blocks to interscalene nerve block for clinical outcomes after shoulder surgery

Detailed Description

In this study, the investigators planned to investigate postoperative pain, analgesic dosage, respiratory effects of the block and side effects of patients undergoing general anaesthesia after arthroscopic shoulder surgery under preoperative interscalene nerve block or suprascapular + infraclavicular nerve block.

Registry
clinicaltrials.gov
Start Date
September 30, 2019
End Date
April 1, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Diskapi Yildirim Beyazit Education and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Tugba Arslan

Principle Investigator

Diskapi Yildirim Beyazit Education and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • •Patients scheduled for elective shoulder surgery under general anesthesia with suprascapular + infraclavicular nerve block or interscalene nerve block for any reason ASA 1-3 patients

Exclusion Criteria

  • •coagulopathy
  • •local anesthetic allergy
  • •chronic opioid users
  • •neurological deficit of the surgical limb
  • •obstructive or restrictive pulmoner disease
  • •inability to understand pain scores

Outcomes

Primary Outcomes

postoperative pain: numeric rating scale (NRS)

Time Frame: postoperative 30. minute, 4. hour, 8.hour,12. hour, 24. hour, 48. hour

postoperative pain will be evaluated by numeric rating scale (NRS) .

Secondary Outcomes

  • phrenic nerve paralysis evaluated with ultrasound(thirty minutes after the nerve block)

Study Sites (1)

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