M-Tapa Block for Laparoscopic Cholesistectomy
Cholecystitis, Cholecystitis, Acute, Cholecystitis, Chronic
About this trial
This is an interventional treatment trial for Cholecystitis focused on measuring Laparoscopic Cholesistectomy, M-Tapa Block, Postoperative Analgesia
Eligibility Criteria
Inclusion Criteria:
- American Society of Anesthesiologists (ASA) classification I-II
- Scheduled for laparoscopic cholesistectomy surgery under general anesthesia
Exclusion Criteria:
- Bleeding diathesis
- Receiving anticoagulant treatment
- Known local anesthetics and opioid allergy
- Infection of the skin at the site of the needle puncture
- Pregnancy or lactation
- Patients who do not accept the procedure
Sites / Locations
- Istanbul Medipol University Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
No Intervention
Group M = M-TAPA group
Group C = Control group
Patients will be administered ibuprofen 400 mgr IV every 8 hours in the postoperative period. Postoperative patient evaluation will be performed by a pain nurse blinded to the procedure. 100 mg tramadol will be performed for rescue analgesia.
Patients will be administered ibuprofen 400 mgr IV every 8 hours in the postoperative period. Postoperative patient evaluation will be performed by a pain nurse blinded to the procedure. Wound local anesthetic infiltration will be applied to the patients in the control group. 100 mg tramadol will be performed for rescue analgesia.