CoreSys Monitoring for Intraoperative Stress Management in Abdominal Hysterectomy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-70
SponsorHospital Provincial de Rosario

About this trial

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.

Eligibility criteria

Qualifiers

Female patients aged 18-70 years

Scheduled elective open abdominal hysterectomy in the morning

Written informed consent

Disqualifiers

Refusal to participate

Significant endocrine/metabolic disease

Pacemaker or major arrhythmias

Contraindication to epidural anesthesia

Trial design

Treatments tested in this trial

  • propofol
  • CoreSys Monitor
  • Remifentanil (Target-Controlled Infusion)

Treatment groups

30 Participants
are divided into 2 treatment groups

Sponsors and collaborators