Clinical Trial

Propofol vs Remifentanil for Sedation in Gastroscopy

Study acronym: ROPOGAST
Completed
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Summary
This prospective randomized study aims to compare propofol and remifentanil for sedation during elective diagnostic gastroscopy. The ideal sedative agent for gastroscopy should provide adequate sedation, rapid recovery, patient safety, and high endoscopist satisfaction. Although propofol is widely used for procedural sedation, remifentanil's ultra-short pharmacokinetic profile may offer advantages in short procedures such as gastroscopy. However, comprehensive comparative data evaluating recovery quality, safety, and procedural conditions between these agents remain limited. This study evaluates sedation efficacy, recovery characteristics, complication rates, and endoscopist satisfaction associated with propofol- and remifentanil-based sedation protocols.
Protocol Amendment History 1 change
critical Trial completed 2026-04-22
Trial Details
NCT Number NCT07336628
Lead Sponsor Fatih Sultan Mehmet Training and Research Hospital
Conditions Conscious Sedation, Procedural Sedation
Enrollment 80 participants
Start Date 2026-02-02
Primary Completion 2026-04-01 (estimated)
Study Completion 2026-04-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-21