This study investigates the effectiveness of different pain management strategies for patients undergoing minimally invasive abdominal cancer surgery. The focus is on comparing various approaches to control pain during and after surgery.
The purpose of this study is to evaluate the effectiveness and safety of different pain management techniques. Researchers will assess how well each method works to control pain after surgery.
- Who can participate: Adults aged 18 to 89 scheduled for elective minimally invasive oncologic surgery who can understand and report pain using a visual scale may participate. Participants must have an ASA classification of I, II, or III and provide informed consent.
- Study details: Participants will be randomly assigned to one of three pain management strategies during surgery. Data will be collected for 24 hours post-surgery and upon hospital discharge.
- Study timelines: Participation in the study will end upon discharge from the hospital.
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