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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UNKNOWN
34 participants
OBSERVATIONAL
2020-09-02
2021-09-02
Brief Summary
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Detailed Description
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In the intraoperative period, 10 mg / kg paracetamol and 0.05 mg / kg morphine will be used for postoperative analgesia. After surgery, all patients will be given 10 mg/kg paracetamol every 8 hours and will be fitted with a patient-controlled analgesia (PCA) device (Tramadol HCL). PCA device bolus dose will be set to 20 mg, lock time will be set to 10 minutes and the number of buttons per hour will be set as 3.for postoperative analgesia.After surgery, VAS scores of the patients will be evaluated (in the recovery room, 1,3,6,12 and 24 hours, Patients with VAS≥4 will be given 0.03mg / kg morphine as salvage analgesia.After 30 minutes, the patients' VAS will be re-evaluated,If VAS≥4 the same dose will be repeated.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Interventions
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Block group
Patients received lumbar erector spinae plane Block before operation
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Tokat Gaziosmanpasa University
OTHER
Responsible Party
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Hakan Tapar
Tokat Gaziosmanpasa University
Principal Investigators
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Hakan Tapar
Role: PRINCIPAL_INVESTIGATOR
Gaziosmanpasa University
Locations
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Gaziosmanpasa University
Tokat Province, , Turkey (Türkiye)
Countries
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Central Contacts
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Other Identifiers
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19-KAEK-129
Identifier Type: -
Identifier Source: org_study_id
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