CoreSys Monitoring for Intraoperative Stress Management in Abdominal Hysterectomy
Recruiting
N/A
Interventional Study
Surgical Stress Response
Inflammation
Anesthesia
Perioperative Care
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 70
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 30 (estimated)
- Sponsor
- Hospital Provincial de Rosario · Other
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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 conven…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Female patients aged 18-70 years
* Scheduled elective open abdominal hysterectomy in the morning
* Written informed consent
Exclusion Criteria:
* Refusal to participate
* Significant endocrine/metabolic disease
* Pacemaker or major arrhythmias
* Contraindication to epidural …
Contacts