Monitoring Analgesia by ANI (Analgesia The Nociception Index)

University Hospital, Lille25 enrolled

Overview

The objective of this research is to study the variations of the ANI(Analgesia The Nociception Index) according to 2 periods: the "NoStim" period before surgical incision under general anesthesia and the period of hemodynamic reactivity "ReactHemo" peroperative. This period is defined by a 20% increase in FC and / or PAS (the only gold standard today).

Study Type

INTERVENTIONAL

Allocation

Purpose

DIAGNOSTIC

Masking

NONE

Enrollment

Conditions

Nociceptive Pain Surgical Procedure, Unspecified

Interventions

ANI monitorDEVICE

experimental medical device using expert rules and continuous reading of heart rate, blood pressure and Analgesia Nociception Index

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * patient with IBD * Scheduled surgery: laparotomy or laparoscopic resection with high risk of laparo-conversion Exclusion Criteria: * patient included in another current study or the previous month * urgent surgery * toxicomania or receiving opioids preoperatively * pregnant woman * psychosis * betablocker treatment * diabetic dysautonomia * non-sinus heart rate * pacemaker heart transplant

Locations (1)

Hôpital Claude Huriez, CHU

Lille, France

Outcomes

Primary Outcomes

Change of ANI greater than 20 points

ANI decrease greater than 20 points between a "NoStim" period before surgical incision under general anesthesia and a period of intraoperative "ReactHemo" hemodynamic reactivity defined by a 20% increase in FC and / or PAS.

Time frame: During the surgery, an average Three hours and a half

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.