About this trial
This prospective observational study aims to compare the effects of bilateral ultrasound-guided recto-intercostal plane block(RIPB) and bilateral ultrasound-guided external oblique intercostal plane block(EOIPB) on postoperative analgesia in patients undergoing elective laparoscopic cholecystectomy under general anesthesia.
Both blocks are performed after anesthesia induction as part of routine preemptive multimodal analgesia practice. Patients who receive bilateral recto-intercostal plane block will be included in the RIPB group, and patients who receive bilateral external oblique intercostal plane block will be included in the EOIPB group.
The primary outcome is cumulative intravenous tramadol consumption via patient-controlled analgesia during the first 24 postoperative hours. Secondary outcomes include postoperative pain scores at rest and during activity, rescue analgesic requirement, postoperative nausea and vomiting, time to mobilization, length of hospital stay, quality of recovery assessed using the Quality of Recovery-15 questionnaire, and block-related complications.
Eligibility criteria
Qualifiers
Age between 18 and 75 years
American Society of Anesthesiologists (ASA) physical status I-III
Scheduled for elective laparoscopic cholecystectomy under general anesthesia
Written informed consent obtained
Disqualifiers
Refusal to participate
Inability to understand the study protocol or provide informed consent
Known allergy to local anesthetics, tramadol, paracetamol, dexketoprofen, or other study drugs
Chronic opioid or steroid use
Trial design
Treatments tested in this trial
- Bilateral Ultrasound-Guided Recto-Intercostal Plane Block
- Bilateral Ultrasound-Guided External Oblique Intercostal Plane Block