drugset / Trial / NCT07571473

CoreSys Monitoring for Intraoperative Stress Management in Abdominal Hysterectomy

NCT07571473 ↗

RandomizedParallel-groupSingle-blindTreatment

Summary

This randomized controlled trial evaluates whether intraoperative guidance using the CoreSys monitor reduces the surgical stress response in patients undergoing elective open abdominal hysterectomy. Surgical stress involves complex hemodynamic, endocrine, and inflammatory responses that may negatively impact postoperative recovery. Patients will be randomized to either anesthesia guided by conventional clinical and hemodynamic parameters or anesthesia additionally guided by CoreSys-derived indices of consciousness, nociception, and stress activity. The primary objective is to assess whether CoreSys-guided anesthesia attenuates stress biomarkers, including interleukin-6 (IL-6), cortisol and glycemia.

Timeline

Start
2025-01-08
Primary completion
2026-05-30
Completion
2026-05-30

Drugs

EvaluationDrugModalityDoseRoute
Background Propofol Small molecule — Intravenous
Background Remifentanil Small molecule — Intravenous

Indications

No indication recorded.