Impact of Intraoperative Non-invasive Analgesia Monitoring Using Nociception Level Index on Patient Management
Recruiting
N/A
Interventional Study
Pain
Anesthesia
Perioperative Care
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 160 (estimated)
- Sponsor
- Osoian Cristiana · Other
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About This Trial
This prospective randomised clinical trial aims to assess the impact of intraoperative nociception monitoring using NOL on anesthetic management during major abdominal surgery. Additionally, the study will objectively evaluate using NOL how intravenous lidocaine administration, influences opioid requirements and the effect of this multimodal approach on early postoperative outcomes. The investigat…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* age \> 18 years
* ASA score I-III
* surgery for gastric or hepatobiliary or pancreatic neoplasia
Exclusion Criteria:
* pregnancy
* lactation
* neuraxial or regional anesthesia
* chronic treatment with drugs that can influence autonomic nervous system
* diuretics or nitroglyc…
Contacts