Clinical Trial

EVALUATION OF POSTOPERATIVE NEUROCOGNITIVE IMPAIRMENT

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Record status
This record was last updated November 14, 2024 (before its estimated February 15, 2025 completion). Its status may not reflect the trial's current state.
Summary
In this prospective study, the effects of different anesthesia methods (total intravenous anesthesia and inhaled anesthesia) on neurocognitive function will be examined in patients undergoing breast-conserving surgery without axillary lymph node dissection. Mini-Mental State Examination and Mini-Cog tests will be administered at specific intervals pre and postoperatively. Anesthesia management will follow standard protocols, and the researcher will not intervent in these processes. The relationship between the type of anesthesia and neurocognitive outcomes will be evaluated based on the collected data.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-11-11.
Trial Details
NCT Number NCT06685770
Lead Sponsor Haseki Training and Research Hospital
Conditions Neurocognitive Disorder, General Anesthesia, Total Intravenous Anesthesia, Sevoflurane Anaesthesia, Breast Surgery
Enrollment 80 participants
Start Date 2024-11-12
Primary Completion 2025-02-15 (estimated)
Study Completion 2025-05-15 (estimated)
Updated on ClinicalTrials.gov 2024-11-14