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NCT03694626

Objectively Diagnose and Monitor Treatment of Light Sensitivity

Recruiting now NA Last updated 24 November 2025
What this trial tests

NA trial testing Pupillography in Photophobia in 120 participants. Currently enrolling.

Timeline
11 July 2019
Primary endpoint
1 January 2028
1 January 2028

Quick facts

Lead sponsorRandy Kardon
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposescreening
Enrollment120
Start date11 July 2019
Primary completion1 January 2028
Estimated completion1 January 2028
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Randy Kardon

Who can join

Adults 18 to 80, any sex, with Photophobia or Traumatic Brain Injury. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Pupillography

Trials testing the same drug.

Other recruiting trials for Photophobia

Currently open trials in the same condition.

Other Randy Kardon trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03694626.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing