Efficacy and Safety of Superior Trunk Block Versus Interscalene Block for Post-operative Analgesia in Shoulder Surgeries
NCT ID: NCT05978427
Last Updated: 2024-06-28
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
40 participants
INTERVENTIONAL
2023-05-01
2023-12-01
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
TREATMENT
QUADRUPLE
Study Groups
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interscalene block group
participants undergoing shoulder surgeries will receive ultrasound guided interscalene block
interscalene block
will receive a 20 ml mixture of local anesthetic solution prepared as 10 ml of bupivacaine 0.5% diluted with 10 ml normal saline 0.9% will be injected in interscalene block.
superior trunk block
will receive a 20 ml mixture of local anesthetic solution prepared as 10 ml of bupivacaine 0.5% diluted with 10 ml normal saline 0.9% will be injected in superior trunk block.
superior trunk block group
participants undergoing shoulder surgeries will receive ultrasound guided superior trunk block
interscalene block
will receive a 20 ml mixture of local anesthetic solution prepared as 10 ml of bupivacaine 0.5% diluted with 10 ml normal saline 0.9% will be injected in interscalene block.
superior trunk block
will receive a 20 ml mixture of local anesthetic solution prepared as 10 ml of bupivacaine 0.5% diluted with 10 ml normal saline 0.9% will be injected in superior trunk block.
Interventions
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interscalene block
will receive a 20 ml mixture of local anesthetic solution prepared as 10 ml of bupivacaine 0.5% diluted with 10 ml normal saline 0.9% will be injected in interscalene block.
superior trunk block
will receive a 20 ml mixture of local anesthetic solution prepared as 10 ml of bupivacaine 0.5% diluted with 10 ml normal saline 0.9% will be injected in superior trunk block.
Eligibility Criteria
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Inclusion Criteria
* Both genders.
* Aged group from 21 to 50 years old.
* Patients electively scheduled for shoulder surgery under general anesthesia with normal coagulation profile.
Exclusion Criteria
* Any history or evidence of coagulopathy.
* Evidence of infection at injection site.
* Allergy to study drugs.
* Patients with pulmonary severe respiratory disease.
* Herniated cervical disc or cervical myelopathy.
* Pre-existing neuropathy of the operative limb
21 Years
50 Years
ALL
Yes
Sponsors
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Ain Shams University
OTHER
Responsible Party
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Locations
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Ainshams University
Cairo, , Egypt
Countries
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Other Identifiers
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superior trunk vs interscalene
Identifier Type: -
Identifier Source: org_study_id
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