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
NA
60 participants
INTERVENTIONAL
2020-02-01
2021-01-02
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
DOUBLE
Study Groups
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Group USP
The group using ultrasound and injection pressure manometer was named USP
fentanyl will be added
If adequate anagesia is not provided with the block, 1 microgram/kg of fentanyl will be added
general anesthesia
If adequate anagesia is not provided with the block, general anesthesia will be administered.
Group USPN
The group using ultrasound , injection pressure manometer , and neurostimulator was named USPN
fentanyl will be added
If adequate anagesia is not provided with the block, 1 microgram/kg of fentanyl will be added
general anesthesia
If adequate anagesia is not provided with the block, general anesthesia will be administered.
Interventions
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fentanyl will be added
If adequate anagesia is not provided with the block, 1 microgram/kg of fentanyl will be added
general anesthesia
If adequate anagesia is not provided with the block, general anesthesia will be administered.
Eligibility Criteria
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Inclusion Criteria
* being between 18 and 80 years of age,
* body mass index (BMI) between 18 and 35 kg/m2
Exclusion Criteria
* were above ASA III,
* pregnant,
* had a neuromuscular disease,
* bleeding diathesis,
* a local anesthetic allergy,
* an infection in the area where nerve block would be applied, and
* had previously operated from the infraclavicular fossa were not included in the study
18 Years
80 Years
ALL
No
Sponsors
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Gaziosmanpasa Research and Education Hospital
OTHER_GOV
Responsible Party
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Döndü Genc Moralar
Associate Professor
Locations
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Gazoosmanpasa Education and Research Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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Neurostimulator Usage
Identifier Type: -
Identifier Source: org_study_id
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