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Can your eyes reveal pain? new device aims to end opioid guesswork
NCT ID NCT03605966
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a device that uses changes in pupil size to measure pain and how well opioid painkillers are working. The goal is to replace subjective pain scores with an objective measurement, helping doctors prescribe opioids more safely. The study includes 40 children and young adults aged 7 to 21 who are already receiving opioids for pain. Researchers will compare pupil reflex data before and after opioid doses to see if the device can accurately detect pain type and drug effectiveness.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2018
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants who are receiving opioid as part of their standard care will be recruited from the Inpatient Pain at Children's National Medical Center (CNMC).
- Ages
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7 to 21 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. The subject is 7 to 21 years of age 2. The subject is receiving an opioid via bolus or a patient controlled analgesia (PCA) apparatus as part of treatment or fentanyl infusion in the pediatric intensive care unit (PICU) (generally postoperative patients). 3. The subject is willing and able to provide written informed assent/parental consent to study participation Exclusion Criteria: 1. Eye pathology precluding pupillometry 2. For patients in the PICU, patients who are hemodynamically unstable
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Children's National Health System
Washington D.C., District of Columbia, 20010, United States