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Not Yet RecruitingNCT07145762

Analgesia Nociception Index In Pediatric Patients With Chronic Pain

Validity of the Analgesia Nociception Index in Children and Adolescents With Chronic Pain

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre · Academic / Other
Sex
All
Age
9 Years – 17 Years
Healthy volunteers
Not accepted

Summary

The goal of this observational study is to learn about the analgesia nociceptive index (ANI) is associated with pain sensitivity in patients between the ages of 9-17 who are experiencing chronic pain. The main question it aims to answer is: \- Does the ANI score correlate with the change in the pain sensitivity in patients aged 9-17 undergoing an interventional block. Patients already receiving an interventional block as part of their regular medical care for chronic pain will have their level of pain recorded during clinic appointments

Conditions

Interventions

TypeNameDescription
PROCEDUREInterventional BlockFor patients who are offered interventional blocks as part of their standard of care, we will measure ANI as well as pressure pain threshold before, during, and after the block as well and at follow-up to assess correlation with treatment efficacy.

Timeline

Start date
2025-09-15
Primary completion
2026-09-01
Completion
2026-10-01
First posted
2025-08-28
Last updated
2025-08-28

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT07145762. Inclusion in this directory is not an endorsement.