Clinical Trial

Comparison of Target-Controlled and Manual Total Intravenous Anesthesia in Supratentorial Surgery

Recruiting
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Record status
This record was last updated March 25, 2026 (before its estimated May 2026 completion). Its status may not reflect the trial's current state.
Summary
This study aims to investigate the effect of target-controlled infusion using the Eleveld pharmacokinetic model compared with manually controlled total intravenous anesthesia on the incidence of postoperative delirium in patients undergoing supratentorial surgery. Propofol and remifentanil are administered using either target-controlled or manual infusion techniques according to the study protocol. Secondary objectives include comparisons of intraoperative anesthetic consumption, hemodynamic responses, recovery profiles, postoperative pain, and postoperative nausea and vomiting between the two anesthesia strategies. The study seeks to evaluate whether target-controlled infusion provides improved anesthetic management and postoperative outcomes compared with manual total intravenous anesthesia.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-01-21.
Status change: Not Yet Recruiting → Recruiting 2026-03-24
Trial Details
NCT Number NCT07357480
Lead Sponsor Istanbul University - Cerrahpasa
Conditions Postoperative Delirium (POD), Postoperative Pain, PONV, Burst Suppression, Recovery Period, Anesthesia
Enrollment 70 participants
Start Date 2026-01-14
Primary Completion 2026-05 (estimated)
Study Completion 2026-05 (estimated)
Updated on ClinicalTrials.gov 2026-03-25