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Clinical Trials/NCT04101266
NCT04101266CompletedNot 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 enrollmentStarted: September 30, 2019Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
76
Locations
1
Primary Endpoint
postoperative pain: numeric rating scale (NRS)
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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)

Investigators

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

Tugba Arslan

Principle Investigator

Diskapi Yildirim Beyazit Education and Research Hospital

Study Sites (1)

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