The goal of this clinical trial is to learn if intravenous dexamethasone can help prolong the effect of spinal anesthesia in adults having elective pelvic, urologic, or proctologic surgery. The study also looks at whether dexamethasone improves pain control after surgery and whether it causes any side effects. The main questions it aims to answer are: Does intravenous dexamethasone increase how long the spinal anesthesia lasts? Does it reduce the need for pain medications after surgery? Does it cause more or fewer side effects compared to a placebo? In this study: Participants were randomly assigned to receive either 8 mg of intravenous dexamethasone or a placebo (salt water). All participants received standard spinal anesthesia with bupivacaine and sufentanil. Researchers measured how long the spinal anesthesia lasted and when the first pain medication was needed after surgery. Participants were monitored for side effects such as low blood pressure, nausea, vomiting, and slow heart rate. Surgeon satisfaction with anesthesia quality was also recorded. Participants did not receive any additional procedures beyond routine care. The study found that dexamethasone helped prolong the spinal anesthesia and delayed the need for pain relief, without increasing side effects.
Age range
18 Years – 80 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.
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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.
Duration of sensory block
Timeframe: From the time of spinal injection until sensory regression to L1 dermatome (up to 4 hours postoperatively)