The aim of this clinical trial is to assess preemptive oral pregabalin administration in the obese patients undergoing laparoscopic sleeve gastrectomy. The main aims of the study are to evaluate postoperative pain treatment and effect on the intraoperative hemodynamical stability. The participants will be divided into 2 groups: with or without preemptive pregabalin administration.
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Total postoperative oxycodone consumption
Timeframe: Day "0"
Postoperative pain score in NRS scale
Timeframe: Day "0", assessed 1 hour after operation
Postoperative pain score in NRS scale
Timeframe: Day "0", assessed 6 hour after operation
Postoperative pain score in NRS scale
Timeframe: Day "0", assessed 12 hour after operation
Postoperative pain score in NRS scale
Timeframe: Day "0", assessed 24 hour after operation