Two Different Blocks for Postoperative Analgesia in Patients Undergoing Unilateral Total Knee Arthroplasty
NCT ID: NCT04286035
Last Updated: 2020-03-13
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
PHASE4
70 participants
INTERVENTIONAL
2019-04-02
2019-10-01
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
DOUBLE
Study Groups
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Femoral group
Bupivacaine Injection
Femoral nerve block with 20 ml %0.375 bupivacaine
Adductor group
Bupivacaine Injection
Adductor canal block with 20 ml %0.375 bupivacaine
Interventions
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Bupivacaine Injection
Femoral nerve block with 20 ml %0.375 bupivacaine
Bupivacaine Injection
Adductor canal block with 20 ml %0.375 bupivacaine
Eligibility Criteria
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Inclusion Criteria
* Age: \<55 years
* Unilateral total knee arthroplasty
Exclusion Criteria
* Pregnant
* Emergency
* ASA III-IV
* History of local anesthetic allergy
* Infection in the block area
* Coagulation disorder
* Morbid obesity (body mass index\> 40 kg / m²)
* Severe organ failure
* Previous neurological deficit
* Psychiatric disease
* History of chronic pain
55 Years
ALL
Yes
Sponsors
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Sisli Hamidiye Etfal Training and Research Hospital
OTHER
Responsible Party
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Kerim Şahin
Research assistant
Locations
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SBÜ Şişli Hamidiye Etfal Eğitim ve Araştırma Hastanesi
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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SK01
Identifier Type: -
Identifier Source: org_study_id
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