Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT03694626

Objectively Diagnose and Monitor Treatment of Light Sensitivity

Led by Randy Kardon · Updated on 2025-11-24

120

Participants Needed

1

Research Sites

442 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this project is to provide a new framework for diagnosing and monitoring treatment of light sensitivity and headache by objective measurement of facial features, pupil responses, retinal electrical responses and autonomic nerve responses to light.

CONDITIONS

Official Title

Objectively Diagnose and Monitor Treatment of Light Sensitivity

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 80 years
  • Healthy individuals with a normal eye exam within the past year (for healthy control group)
  • Traumatic Brain Injury (TBI) patients aged 18 to 80 without photosensitivity or headache
  • Patients aged 18 to 80 with photosensitivity symptoms, with or without an identified cause
  • Patients aged 18 to 80 with photosensitivity related to post-traumatic brain injury
Not Eligible

You will not qualify if you...

  • History of eye or systemic disorders affecting the retina, optic nerve, visual pathway, or pupil, including glaucoma, optic neuropathy, retinal disease, or uncontrolled diabetes and/or hypertension
  • History of head trauma, concussion, traumatic brain injury (for certain groups), or cervical/spinal injury or surgery
  • Use of medications or eyedrops that affect pupil light reflex or electromyogram, including topical autonomic drugs, ocular pharmacologic agents, sedatives (e.g., benzodiazepines or barbiturates), or opioid narcotics
  • Being light sensitive or experiencing migraine headaches (for healthy control and certain TBI groups)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Iowa Health Care

Iowa City, Iowa, United States, 52242

Actively Recruiting

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Research Team

J

Julie Nellis, BSN

CONTACT

J

Jan Full, BSN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

5

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Objectively Diagnose and Monitor Treatment of Light Sensitivity | DecenTrialz