Erector Spinae Plane Block for Postoperative Analgesia Management Following Video Assisted Thoracic Surgery
NCT ID: NCT03879148
Last Updated: 2019-05-07
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
2018-09-01
2019-04-30
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
SINGLE
Study Groups
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Erector spinae plane block (Group I)
The ultrasound (US) guided ESPB was performed under aseptic conditions at the level of T5 vertebrae using the GE Vivid Q® US device. A high frequency 12 MHz linear US probe was covered with a sterile sheath and placed longitudinally 2-3 cm lateral to the T5 transvers process. After visualizing trapezius, rhomboid major, erector spinae muscles superficial to the hyperechoic transverse process shadow respectively, a 22-gauge 50 mm block needle (Braun Stimuplex Ultra 360, Germany) was inserted in a cephalad to caudad direction. Once the needle tip had been placed within the interfacial plane below the erector spinae muscle, 2 mL of saline were injected to confirm the proper injection site, and then a 20 mL dose of 0.25% bupivacaine was injected. Patients received fentanyl via a patient controlled analgesia (PCA) device with a protocol of 2 mL (10 µg/mL) bolus without an infusion dose, 20 min lockout time and 4 hour limit
Erector spinae plane block
Erector spinae plane block was performed to the patients under aseptic conditions
Control group (Group II)
Patients in control group only received fentanyl via a patient controlled analgesia (PCA) device with a protocol of 2 mL (10 µg/mL) bolus without an infusion dose, 20 min lockout time and 4 hour limit.
No interventions assigned to this group
Interventions
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Erector spinae plane block
Erector spinae plane block was performed to the patients under aseptic conditions
Eligibility Criteria
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Inclusion Criteria
* Must be undergoing VATS lobectomy under general anesthesia
* Must be in American Society of Anesthesiologists (ASA) classification I-II status
Exclusion Criteria
* History of receiving anticoagulant treatment,
* History of local anesthetics or opioid allergy,
* Skin infection at the site of the needle puncture,
* Presence of pregnancy or lactation, and
* Patients who did not accept the procedure
18 Years
65 Years
ALL
No
Sponsors
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Medipol University
OTHER
Responsible Party
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Bahadir Ciftci
Principal Investigator
Locations
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Istanbul Medipol University Hospital
Istanbul, Bagcilar, Turkey (Türkiye)
Countries
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References
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Forero M, Adhikary SD, Lopez H, Tsui C, Chin KJ. The Erector Spinae Plane Block: A Novel Analgesic Technique in Thoracic Neuropathic Pain. Reg Anesth Pain Med. 2016 Sep-Oct;41(5):621-7. doi: 10.1097/AAP.0000000000000451.
Gurkan Y, Aksu C, Kus A, Yorukoglu UH, Kilic CT. Ultrasound guided erector spinae plane block reduces postoperative opioid consumption following breast surgery: A randomized controlled study. J Clin Anesth. 2018 Nov;50:65-68. doi: 10.1016/j.jclinane.2018.06.033. Epub 2018 Jul 2.
Nagaraja PS, Ragavendran S, Singh NG, Asai O, Bhavya G, Manjunath N, Rajesh K. Comparison of continuous thoracic epidural analgesia with bilateral erector spinae plane block for perioperative pain management in cardiac surgery. Ann Card Anaesth. 2018 Jul-Sep;21(3):323-327. doi: 10.4103/aca.ACA_16_18.
Other Identifiers
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Medipol University Hospital
Identifier Type: -
Identifier Source: org_study_id
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