Validation of the ANI in Perpubescent Patients in Pediatric Intensive Care Unit.

Last updated: December 18, 2025
Sponsor: University Hospital, Lille
Overall Status: Completed

Phase

N/A

Condition

Pain

Treatment

N/A

Clinical Study ID

NCT04913038
2020_92
2021-A00487-34
  • Ages 2-12
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

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

Exclusion

Exclusion Criteria:

  • Non sinusal rythm

  • Atropine

  • Pace-macker

Study Design

Total Participants: 50
Study Start date:
June 29, 2021
Estimated Completion Date:
November 23, 2023

Connect with a study center

  • Hop Jeanne de Flandre Chu Lille

    Lille, 59037
    France

    Site Not Available

  • Hop Jeanne de Flandre Chu Lille

    Lille 2998324, 59037
    France

    Site Not Available

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