The Analgesic Efficacy Supra-scapular Nerve RF After Breast Surgery
NCT ID: NCT03247842
Last Updated: 2020-06-16
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
80 participants
INTERVENTIONAL
2017-04-25
2019-06-30
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
SUPPORTIVE_CARE
QUADRUPLE
Study Groups
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suprascapular nerve RF
Eighty patients with chronic shoulder pain after breast surgery were allocated randomly into 2 groups (Figure1); forty patients received fluoroscopically guided supra-scapular nerve pulsed radiofrequency (PRF) followed by injection through the radiofrequency needle of mL of 0.25% bupivacaine solution containing 40 mg of methylprednisolone (group1)
suprascapular nerve block
Sixty patients with shoulder dystocia after breast surgery will receive stellate ganglion neurolysis with supra-scapular nerve radiofrequency,
suprascapular nerve block
and forty patients received fluoroscopically guided supra-scapular nerve injection of mL of 0.25% bupivacaine solution containing 40 mg of methylprednisolone (group 2) without active pulsed radiofrequency only demo mode was applied.
suprascapular nerve block
Sixty patients with shoulder dystocia after breast surgery will receive stellate ganglion neurolysis with supra-scapular nerve radiofrequency,
Interventions
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suprascapular nerve block
Sixty patients with shoulder dystocia after breast surgery will receive stellate ganglion neurolysis with supra-scapular nerve radiofrequency,
Eligibility Criteria
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Inclusion Criteria
18 Years
60 Years
FEMALE
No
Sponsors
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Tanta University
OTHER
Responsible Party
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Ayman Abd Al-maksoud Yousef
assistant professor
Locations
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Tanta university hospital
Cairo, , Egypt
Countries
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Other Identifiers
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3024/01/15
Identifier Type: -
Identifier Source: org_study_id
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