The Effect of Double Injection Erector Spinae Plane Block on Postoperative Pain Following Breast Surgery
NCT ID: NCT03415646
Last Updated: 2018-03-09
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
50 participants
INTERVENTIONAL
2018-02-03
2018-03-07
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
PREVENTION
SINGLE
Study Groups
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Block Group
Erector Spinae Plane Block administered group
Erector Spinae Plane Block
erector spinae plane block with double level injection will be administered before the surgery
Intravenous Morphine patient controlled analgesia device
24 hour morphine consumption will be recorded
Control Group
Control group
Intravenous Morphine patient controlled analgesia device
24 hour morphine consumption will be recorded
Interventions
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Erector Spinae Plane Block
erector spinae plane block with double level injection will be administered before the surgery
Intravenous Morphine patient controlled analgesia device
24 hour morphine consumption will be recorded
Eligibility Criteria
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Inclusion Criteria
* ASA I-II
* Undergoing elective breast cancer surgery
Exclusion Criteria
* infection of the skin at the site of needle puncture area
* patients with known allergies to any of the study drugs
* coagulopathy
* recent use of analgesic drugs.
25 Years
70 Years
FEMALE
No
Sponsors
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Kocaeli University
OTHER
Responsible Party
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Can AKSU
Assistant Professor
Locations
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Kocaeli University Hospital
İzmit, Kocaeli, Turkey (Türkiye)
Countries
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Other Identifiers
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2017-377
Identifier Type: -
Identifier Source: org_study_id
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