Comparison of the Effectiveness of Two Different Block in the Management of Postoperative Analgesia After Lumbar Spinal Surgery
The Effect of Two Different Block Methods on Postoperative Pain Management in Lumbar Spinal Surgery

About this trial
This is an interventional treatment trial for The Effect of Two Different Block Methods on Postoperative Pain Management in Lumbar Spinal Surgery focused on measuring Lumbar spinal surgery, Postoperative pain, QL2 block, TLIP block
Eligibility Criteria
Inclusion Criteria:
- 18-65 years old
- ASA 1-2
Exclusion Criteria:
- Bleeding diathesis
- Opioid allergy
- Infection in the area to be blocked
- Have had previous lumbar surgery
- Pregnant or suspected of pregnancy, breastfeeding
- Gabapenthinoid, corticosteroid users
- Those with kidney failure
- Those with liver failure
- Patients who cannot use a patient-controlled analgesia device
Sites / Locations
- SAMSUN UNIVERSITY Samsun Training and research hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
QL2 block
TLIP block
Posterior QLB process After aseptic conditions are provided, the convex US probe will be covered with a sterile sheath, and an 80-100 mm block needle will be used. After imaging the abdominal muscles with the anterior approach, the needle will be advanced in the Petit triangle and 1-2 ml of saline will be injected into the posterior border of the quadratus lumborum muscle. After the block location is confirmed, 20 ml of local anesthetic infiltration at a concentration of 0.25% will be applied. The same procedure will be applied to the other side. A total of 30 ml of local anesthetic solution will be used.
Classic TLIP block After providing aseptic conditions, the high frequency linear US probe will be covered with a sterile sheath, and a 50 mm block needle will be used. The ultrasound probe will be placed vertically at the level of the L3 vertebra. After visualizing the guiding point spinous process and interspinal muscles, the probe will be moved laterally to visualize the longissimus and multifidus muscles. By using the in-plane technique, the block needle will be directed from medial to lateral, and after reaching the interfacial area between the longissimus and multifidus muscles, the block area will be confirmed by administering 5 ml of serum physiologically. Then, 20 ml of 0.25% local anesthetic will be administered. The same procedure will be applied to the other side. A total of 40 ml of local anesthetic solution will be used.