Bupivacaine With or Without Dexmedetomidine for Postoperative Pain Relief in Abdominal Surgery

Recruiting N/A Interventional Study
Pain, Postoperative
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
21 – 45
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
80 (estimated)
Sponsor
Sheikh Zayed Medical College · Government
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About This Trial
This study investigates the effectiveness of adding dexmedetomidine to bupivacaine for postoperative analgesia in patients undergoing abdominal surgeries. The research compares pain relief in two groups: one receiving a combination of bupivacaine and dexmedetomidine via a transversus abdominis plane (TAP) block, and the other receiving bupivacaine alone. The study aims to evaluate whether dexmedet…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Age between 21 to 45 years. 2. Undergoing elective abdominal surgery (exploratory laparotomy, ileostomy reversal, laparoscopic/open cholecystectomy, mesh repair of paraumbilical hernias). 3. The patient must be capable of providing informed consent. Exclusion Criteria: 1. P…
Contacts

Rameesha Musharaf, FCPS ANESTHESIA (PGR)

0092-334-5038000

rameeshamusharaf96@gmail.com

CONTACT