Effect of Two Different Plane Blocks on Post-thoracotomy Pain
NCT ID: NCT05083832
Last Updated: 2024-03-06
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
60 participants
INTERVENTIONAL
2021-06-09
2024-02-20
Brief Summary
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In this study, the investigators aimed to evaluate the effect of continuous ESPB and continuous SAPB via US-guidance on post-thoracotomy pain.
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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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Continuous erector spinae plane block
Following the visualization of the anatomical structures, the nerve block needle was advanced via the in-plane technique beneath the erector spinae muscles until the interfascial space was reached. After hydrodissection with 2 ml normal saline, 20 ml 0.25% bupivacaine was injected into the area. A catheter will be placed in this area. Then, 5 ml/hour 0.125% bupivacaine will be infused via erector spinae plane block catheter.
Continuous Erector Spina Plane Block vs Continuous Serratus Anterior Plane Block
Two different catheter techniques with same doses local anesthetic infusion
Continuous serratus anterior plane block
Following the visualization of the anatomical structures, the nerve block needle was advanced via the in-plane technique beneath the serratus anterior muscles until the fourth rib area. After hydrodissection with 2 ml normal saline, 20 ml 0.25% bupivacaine was injected into the area. A catheter will be placed in this area. Then, 5 ml/hour 0.125% bupivacaine will be infused via serratus anterior plane block catheter.
Continuous Erector Spina Plane Block vs Continuous Serratus Anterior Plane Block
Two different catheter techniques with same doses local anesthetic infusion
Interventions
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Continuous Erector Spina Plane Block vs Continuous Serratus Anterior Plane Block
Two different catheter techniques with same doses local anesthetic infusion
Eligibility Criteria
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Inclusion Criteria
* ASA physical status I-II-III
* BMI 18 to 30 kg/m2
* Elective thoracotomy surgery
Exclusion Criteria
* Emergency surgery
* History of chronic opioid or analgesic used
18 Years
65 Years
ALL
No
Sponsors
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Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
OTHER
Responsible Party
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Musa Zengin
Principal İnvestigator
Locations
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Ankara Atatürk Chest Disease and Chest Surgery Training and Research Hospital
Keçiören, Ankara, Turkey (Türkiye)
Countries
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Other Identifiers
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E.Kurul-E1-21-1863
Identifier Type: -
Identifier Source: org_study_id
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