Clinical trial Recruiting at 1 site Early Phase 1 Interventional Ages 30 to 90

Optic Nerve Strain in Non-glaucoma Eyes

Official title: Optic Nerve Head Strain in Non-glaucoma Subjects

Run by Johns Hopkins University · NCT07425535 · Data updated 2026-11-12

This study tests how optic nerve strain responds to lowered eye pressure in people without glaucoma to compare with those who have glaucoma.

Quick facts

PhaseEarly Phase 1
Study typeInterventional
Ages30 Years to 90 Years
SexAll
Enrollment30 (estimated)
SponsorJohns Hopkins University
Academic / other
Locations1 site (Baltimore, Maryland)
StatusRecruiting
StartedJune 24, 2026
Main results expectedMarch 1, 2028
Study endsMarch 31, 2028
Registry record updatedJuly 13, 2026
Trial IDNCT07425535 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults over 30 with no history of open-angle glaucoma and normal retinal nerve fiber layer on OCT.

Probably not a fit

Patients with established OAG or imaging contraindications may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The trial uses a non-invasive imaging approach to measure biomechanical strain on the optic nerve at two intra-ocular pressure levels. It involves giving latanoprost to temporarily reduce eye pressure and capturing optic nerve images before and after the drop. Healthy adults over 30 without open-angle glaucoma (OAG) will be scanned, and results will be compared with glaucoma patients using the same methods. The study is conducted at Johns Hopkins with collaboration from the NEI and focuses on baseline biomechanical properties that may influence glaucoma analysis.

Why it matters

Potential benefit: If successful, the study could improve understanding of how glaucoma-related damage relates to baseline biomechanical properties in non-glaucoma eyes.

How similar studies have gone: Previous work in glaucoma research has used similar imaging and IOP-lowering methods, but this exact non-glaucoma control comparison is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults who have no history of OAG
* Have an ocular examination by a glaucoma specialist with no indications of OAG
* Have normal optical coherence tomography findings in the retinal nerve fiber layer.
* Over age 30 will be included from
* Both sexes
* All ethnic groups.
* Optic neuropathy.
* Both suspects and those with glaucoma damage will be included.
* When both eyes meet inclusion and exclusion criteria, both eyes will be included in the study and statistical methods will be used to account for correlations between eyes within the same individual.

Exclusion Criteria:

* in whom sitting in an upright position is impossible due to physical disability
* with ocular media opacity, corneal scarring, cataract or vitreous hemorrhage, that does not allow adequate imaging resolution.
* in whom keeping the eyes open during the imaging procedure is not possible or uncomfortable.
* who cannot perform home tonometry accurately at certification
* who do not have reliable clinical Optical Coherence Tomography (OCT) testing.
* with any form of glaucoma
* with high myopia defined as refractive error \> -8
* with past keratorefractive surgery, corneal dystrophy, or corneal ectasia that would make self-tonometry measurements difficult to interpret
* inability to understand English or with a language or hearing impairment

Where it's running

  • Johns Hopkins Hospital
    Baltimore, Maryland, United States
    Recruiting

Study contacts

  • Principal investigator: Harry Quigley, MD — Johns Hopkins University
  • Study coordinator: Harry A Quigley, MD
  • Email: hquigley@jhmi.edu
  • Phone: 410 955 6051

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.