Ultrasound-guided Erector Spinae Plane Block Versus Retrolaminar Block for Postoperative Analgesia in Thoracotomy
Postoperative Analgesia, Retrolaminar Block, Ultrasound-guided Erector Spinae Plane Block
About this trial
This is an interventional treatment trial for Postoperative Analgesia
Eligibility Criteria
Inclusion Criteria:
- Adult patients aged 21-65 years old of both sexes.
- Patients were scheduled for elective thoracotomy.
- Their ASA physical status classification is II-III.
Exclusion Criteria:
- Patients' refusal.
- Local infection at the site of block.
- Coagulation abnormalities.
- Sever spinal deformity e.g. scoliosis.
- Known hypersensitivity to local anesthetics.
- Mental dysfunction and cognitive disorders.
- History of drug abuse and chronic analgesic use.
Sites / Locations
- Tanta University
Arms of the Study
Arm 1
Arm 2
Arm 3
Sham Comparator
Experimental
Experimental
Control group
Ultrasound-guided Erector Spinae Plane Block
Retrolaminar Block
Patients received general anesthesia alone.
A 22-gauge needle is inserted at a puncture site lateral to the target spinous process using ultrasound imaging and advanced until contact is made with the transverse process. The local anesthetic agent will be injected between the transverse process and the erector spinae muscle using 20 ml (19ml bupivacaine 0.25% plus 1ml dexamethasone 4mg).
A 22-gauge needle is inserted at a puncture site lateral to the target spinous process using ultrasound imaging and advanced caudally or cranially until it contacts the lamina. The local anesthetic agent will be injected on the lamina using 20 ml (19ml bupivacaine 0.25% plus 1ml dexamethasone 4mg).