Clinical Trial

Deep Versus Moderate Neuromuscular Blockade in Bariatric Surgery

Not Yet Recruiting
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Summary
The aim of this study is to investigate the effect of depth of neuromuscular blockade on the surgical field, patient postoperative pain, intestinal motility, the incidence of postoperative nausea and vomiting and the effect of deep versus moderate neuromuscular blockade on postoperative atelectasis quantitatively using chest computed tomography.This is a prospective, randomized, controlled clinical-controlled study in patients ≥18 years old scheduled to undergo elective bariatric surgery.
Trial Details
NCT Number NCT06553066
Lead Sponsor University Hospital of Patras
Conditions Neuromuscular Blockade
Enrollment 50 participants
Start Date 2024-08
Primary Completion 2026-08 (estimated)
Study Completion 2026-08 (estimated)
Updated on ClinicalTrials.gov 2024-08-14