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

NCT04913038 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2025-12-19

No results posted yet for this 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.

Conditions

  • Pain
  • Pediatric ALL

Sponsors & Collaborators

  • University Hospital, Lille

    lead OTHER

Principal Investigators

  • Morgan RECHER, MD · University Hospital, Lille

Eligibility

Min Age
2 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-29
Primary Completion
2023-11-22
Completion
2023-11-23

Countries

  • France

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04913038 on ClinicalTrials.gov