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

StatusCompleted
PhaseNot applicable
Started2026-01-14
View on ClinicalTrials.gov ↗

Amendment history

2026-09-05
notable
Study Status, Study Design, Contacts/Locations v2
Trial completed
Final enrollment: 63 participants (planned 70)
Study completion confirmed: July 2026 (last estimated May 2026)
Primary completion dateestimated 2026-05→confirmed 2026-06-07
Completion dateestimated 2026-05→confirmed 2026-07-16
Enrollment targetestimated 70→confirmed 63
Study sitesdetails revised at 2 of 2 sites
2026-03-24
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Start dateestimated 2026-01-12→confirmed 2026-01-14
Study sites1→2
2026-01-21
minor
Original filing
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.
Trial Details
NCT Number NCT07357480
Lead Sponsor Istanbul University - Cerrahpasa
Conditions Postoperative Delirium (POD), Postoperative Pain, PONV, Burst Suppression, Recovery Period, Anesthesia
Enrollment 63 participants
Start Date 2026-01-14
Primary Completion 2026-06-07 (estimated)
Study Completion 2026-07-16 (estimated)
Updated on ClinicalTrials.gov 2026-09-09