US-Guided ESPB Versus TPVB on Acute and Chronic Pain After VATS
NCT ID: NCT04964401
Last Updated: 2021-09-24
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
2021-04-13
2021-09-23
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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Thoracic Paravertebral Block
After the linear ultrasound (US) probe will be placed 2-3 cm lateral to the thoracic 5 spinous process, the US-compatible needle will be advanced to the paravertebral area with in-plane technique, and 20 ml of 0.25% bupivacaine hydrochloride will be injected into this area.
Thoracic paravertebral block vs Erector spinae plane block
Thoracic paravertebral block and erector spinae plane block will be performed unilaterally, under US guidance, before the surgical operation, after the induction of anesthesia, when the patient is placed in the lateral decubitus position.
Erector spinae plane block
After the linear ultrasound (US) probe will be placed 2-3 cm lateral to the T5 spinous process, 20 ml of 0.25% bupivacaine hydrochloride will be injected into the interfacial space below the erector spinae muscle, above the transverse process.
Thoracic paravertebral block vs Erector spinae plane block
Thoracic paravertebral block and erector spinae plane block will be performed unilaterally, under US guidance, before the surgical operation, after the induction of anesthesia, when the patient is placed in the lateral decubitus position.
Interventions
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Thoracic paravertebral block vs Erector spinae plane block
Thoracic paravertebral block and erector spinae plane block will be performed unilaterally, under US guidance, before the surgical operation, after the induction of anesthesia, when the patient is placed in the lateral decubitus position.
Eligibility Criteria
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Inclusion Criteria
* American Society of Anesthesiologists physical status I-II-III
* Body mass index between 18-30 kg/m2
* Patients undergoing elective video assiste thoracoscopic surgery
Exclusion Criteria
* History of chronic analgesic therapy
* History of local anesthetic allergy
* Infection in the intervention area
* Patients with bleeding disorders
18 Years
80 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 investigator
Principal Investigators
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Musa Zengin, MD
Role: PRINCIPAL_INVESTIGATOR
Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
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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2012-KAEK-15:2232
Identifier Type: -
Identifier Source: org_study_id
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