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Study identifier: NCT07285083 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Pain, Postoperative  ·  Sponsor: Sheikh Zayed Medical College

PhaseNA
Planned participants80
Who can joinAll sexes, 21 Years to 45 Years
Healthy volunteersNo

About this study

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 dexmedetomidine enhances pain relief, reduces the need for additional pain medication, and impacts sedation and side effects such as hypotension, bradycardia, and nausea. Conducted at Sheikh Zayed Medical College in Rahim Yar Khan, Pakistan, the trial will involve 80 participants and will measure pain using the Visual Analogue Scale (VAS), along with monitoring other vital parameters and complications over 12 hours post-surgery. The primary objective is to determine if the addition of dexmedetomidine provides superior pain control without significantly increasing side effects.

This description comes directly from the study's public registry record.

Talk to the study team

Rameesha Musharaf, FCPS ANESTHESIA (PGR)  ·  0092-334-5038000  ·  rameeshamusharaf96@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Sheikh Zayed Medical CollegeRahim Yar Khan, Punjab Province, PakistanRecruiting

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Source record: clinicaltrials.gov/study/NCT07285083