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Study identifier: NCT06970678 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Combining Dexmedetomidine Infusion and Paragastric Autonomic Neural Block to Enhance Postoperative Recovery in Patients Undergoing Laparoscopic Sleeve Gastrectomy

Condition: Laparoscopic Sleeve Gastrectomy (LSG)  ·  Sponsor: Alexandria University

PhasePhase 1/Phase 2
Planned participants46
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn if combining Dexmedetomidine infusion and paragastric autonomic neural block will enhance the postoperative recovery of patients undergoing laparoscopic sleeve gastrectomy. The main questions it aims to answer are: Will combining the two techniques (Dexmedetomidine infusion and paragastric autonomic neural block) improve the quality of recovery? Will opioid consumption postoperatively decrease after combining those two techniques? Will the patients be able to start mobilizing sooner after surgery? Will the patient encounter less incidence of nausea and vomiting? Researchers will asses the quality of the patients' recovery by reviewing the Quality of recovery 40 (QoR 40) questionnaire filled by the patients, assessing hemodynamic parameters intra- and postoperatively, recording the opioids consumed by the patients in the postoperative period, recording the time to first mobilization of the patient, and recording the incidence of nausea and vomiting.

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

Talk to the study team

Mai A El-Sayed, Lecturer of Anesthesia  ·  00201287459922  ·  m_mohamed165@alexmed.edu.eg

Always discuss trial participation with your own doctor first.

Locations (1)

Alexandria Main University HospitalAlexandria, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT06970678