Monitoring Analgesia by ANI (Analgesia The Nociception Index) (ANI-MICI)

University Hospital, Lille

Status: Completed

Conditions: Surgical Procedure, Unspecified; Nociceptive Pain

Treatments: Device: ANI monitor

Study type: Interventional

Funder types: Other

Identifiers

NCT03749304

2012-A01363-40 (Other Identifier)

2012_31

Details and patient eligibility

About

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).

Enrollment: 25 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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25 participants in 1 patient group

ANI monitor

Experimental group

Treatment:

Device: ANI monitor