Actively Recruiting

Age: 7Years - 21Years
All Genders
NCT03794362

Measuring Analgesic Interventions

Led by Julia Finkel · Updated on 2026-04-07

120

Participants Needed

1

Research Sites

422 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

It is generally recognized that pain assessment and management especially in newborns, children and other nonverbal populations is an unmet need. According to the American Medical Association, "the pediatric population is at risk of inadequate pain management, with age-related factors affecting pain management in children. Children are often given minimal or no analgesia for procedures that would routinely be treated aggressively in adults. Although much is now known about pain management in children, it has not been widely or effectively translated into routine clinical practice". These two factors combine to emphasize the necessity for an objective tool to quantify pain and monitor the effectiveness of analgesia, especially during treatments. Further, it is reported that many patients require a combination of treatments, and it is often necessary to test a variety of treatments before the personal match for treatment is found. The method in place to change the care on a subjective basis is difficult, time consuming, and not easily individualized. This pilot study is part of an ongoing effort to develop a method to objectively assess response to specific analgesic interventions. It specifically aims to discern the impact of analgesic interventions on sensory nerve fiber sensitivity in a diverse patient population.

CONDITIONS

Official Title

Measuring Analgesic Interventions

Who Can Participate

Age: 7Years - 21Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • The participant is between 7 and 21 years old
  • The participant is receiving an analgesic intervention at the Children's National Medical Center Pain Clinic
  • The participant or parent/guardian is willing and able to provide written informed assent or consent for study participation
Not Eligible

You will not qualify if you...

  • Presence of eye problems that prevent pupillometry
  • Current use of opioid medications (past use allowed)
  • Pregnancy or possible pregnancy

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Children's National Health System

Washington D.C., District of Columbia, United States, 20010

Actively Recruiting

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Research Team

J

Julia C Finkel, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

6

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