About this trial
This single-center, prospective, randomized controlled trial aims to compare the effects of paravertebral block (PVB), external oblique intercostal (EOI) block, and intravenous patient-controlled analgesia (PCA) with tramadol on postoperative pain and opioid consumption in patients undergoing elective laparoscopic cholecystectomy. The primary endpoint is total tramadol consumption within 24 hours postoperatively. Secondary outcomes include pain scores, additional analgesic use, incidence of nausea/vomiting, mobilization time, and length of hospital stay.
Eligibility criteria
Qualifiers
Age between 18 and 65 years
Scheduled for elective laparoscopic cholecystectomy under general anesthesia
ASA physical status I-III
Able to understand the study procedure and provide informed consent
Disqualifiers
None
Trial design
Treatments tested in this trial
- Paravertebral Block (PVB)
- External Oblique Intercostal Block (EOI Block)
- Tramadol IV Patient-Controlled Analgesia (PCA)