Combined Anterior Suprascapular Nerve Block and Superficial Cervical Plexus Block In Shoulder Arthroplasty Surgery
NCT ID: NCT06146179
Last Updated: 2024-12-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
8 participants
OBSERVATIONAL
2023-11-01
2024-05-30
Brief Summary
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Detailed Description
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Data will be collected by examining these pain observation forms and diaphragm thickness measurements.
Conditions
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Keywords
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Group 1
Group 1: Combined Anterior Suprascapular Nerve Block and Superficial Cervical Plexus Block
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Participants who underwent combined anterior suprascapular nerve block and superficial cervical plexus block in reverse shoulder arthroplasty surgery
* Participants aged 18-80
* ASA I-II-III
Exclusion Criteria
* Pediatric individuals under 18 years of age
* Individuals who are pregnant
* Known diaphragmatic paralysis
* Had an allergy or toxicity to local anesthetic agents
* Have an opioid drug allergy
18 Years
80 Years
ALL
No
Sponsors
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Istanbul Medeniyet University
OTHER
Responsible Party
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Ebru Girgin Dinç, MD
Principal Investigator
Principal Investigators
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Ebru Girgin Dinç
Role: STUDY_DIRECTOR
Istanbul Medeniyet University
Locations
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Istanbul Medeniyet University
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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2023/0363
Identifier Type: -
Identifier Source: org_study_id