Validation of the ANI in Perpubescent Patients in Pediatric Intensive Care Unit. (ANI-EP)

University Hospital, Lille

Status: Completed

Conditions: Pediatric ALL; Pain

Study type: Observational

Funder types: Other

Identifiers

NCT04913038

2021-A00487-34 (Other Identifier)

2020_92

Details and patient eligibility

About

The ANI monitor is a medical device allowing to measure the response of the autonomic nervous system to a painful stimulus.

In the pediatric population under general anesthesia, the ANI score can detect failure of locoregional anesthesia; ANI decreases after painful stimulation during surgery, more markedly with smaller doses of Remifentanil.

To date, measurement of ANI in sedated children in pediatric intensive care has not been performed or validated as a method of assessing pain and discomfort.

Enrollment: 50 patients

Sex: All

Ages: 2 to 12 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Prebubescent chilren (up to 2 years old) Admited in PICU Sedated, ventilated

Exclusion criteria

• Non sinusal rythm
• Atropine
• Pace-macker

Trial design

50 participants in 1 patient group

case group

Description:

children over 2 years of age and prepubescent ventilated and sedated in pediatric intensive care.