Para-sartorial Compartment Block in Knee Surgery
Knee Osteoarthritis, Knee Injuries, Knee Disease
About this trial
This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Knee Surgery, Postoperative pain management, Postoperative Analgesia, Parasartorial compartment block
Eligibility Criteria
Inclusion Criteria:
- Patients with ASA classification I-III,
- Aged 18-75 years
- Who will be scheduled for knee surgery under spinal anesthesia.
Exclusion Criteria:
- Patients who have a history of bleeding diathesis,
- Take anticoagulant therapy,
- History of chronic pain before surgery,
- Multiple trauma,
- Who cannot assess their pain,
- Who have been operated under spinal anesthesia,
- Who have an infection in the area and do not accept the procedure
Sites / Locations
- Istanbul Medipol University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Group PSCB = Parasartorial compartment block group
Group C = Control group
After placing the linear ultrasound probe in the middle of the anterior superior line to the patella and spina drug, the probe will be advanced cephalad to visualize the intermediate femoral cutaneous nerve over the satrorious. Then the block will be applied. Three injections will be made with a single needle entry in the same imaging. The procedure will be completed by applying the first injection to the femoral triangle (10 ml of local anesthetic solution), the second injection to the subsartorial region (10 ml of local anesthetic solution) lateral to the femoral artery, and the third injection to the suprasartorial region (10 ml of local anesthetic solution) (total 30 ml of 0.25% solution). concentration bupivacaine). The block location will be confirmed by injecting 2 ml of saline in every three injections.
Wound infiltration will be applied by the surgical team