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
2018-01-01
2020-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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grup R
Unilateral Rhomboid intercostal and subserratus block + intravenous patient-controlled analgesia
RIIS
unilateral Rhomboid intercostal and subserratus block
Tramadol
intravenous patient-controlled analgesia (tramadol)
Group P
intravenous patient-controlled analgesia
Tramadol
intravenous patient-controlled analgesia (tramadol)
Interventions
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RIIS
unilateral Rhomboid intercostal and subserratus block
Tramadol
intravenous patient-controlled analgesia (tramadol)
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* mental incapacity,
* known allergy to the local anesthetics,
* body mass index ≥35 kg/m2
20 Years
65 Years
ALL
No
Sponsors
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Bursa Yuksek Ihtisas Training and Research Hospital
OTHER_GOV
Responsible Party
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Korgün Ökmen
Principal Investigator ,Assoc. PhD. M.D.
Principal Investigators
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Korgün Ökmen, Assoc. PhD.
Role: PRINCIPAL_INVESTIGATOR
Sağlık Bilimleri Üniversitesi Bursa Yüksek İhtisas Eğitim Ve Araştırma Hastanesi
Locations
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Bursa Yuksek Ihtisas Training and Research Hospital
Bursa, , Turkey (Türkiye)
Countries
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Other Identifiers
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2011-KAEK-25
Identifier Type: -
Identifier Source: org_study_id
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