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Not Yet RecruitingNCT07425535

Optic Nerve Head Strain in Non-glaucoma Subjects

Status
Not Yet Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Johns Hopkins University · Academic / Other
Sex
All
Age
30 Years – 90 Years
Healthy volunteers
Accepted

Summary

Persons who do not have glaucoma will have pictures taken of the optic nerve with a standard camera before and 2 weeks after starting to take a daily glaucoma eye drop to lower eye pressure. These data will be used to compare to the same procedure performed with glaucoma patients to study how glaucoma injures the eye.

Detailed description

The present proposal seeks to measure biomechanical strains in age-matched control subjects who do not have Open-angle Glaucoma (OAG), using the same non-invasive imaging methods as in the above programs. This is necessary as even undamaged OAG eyes may have different biomechanical properties at baseline than do non-OAG eyes. While there are some limited methods to test strains in control eyes, to compare normal to OAG responses robustly, the same methods of changing intra-ocular pressure (IOP) must be applied-namely to lower IOP by delivery of FDA-approved agent, latanoprost, as has been done in the investigator's OAG subjects. The method of measuring strain requires images taken at two different IOP levels.

Conditions

Interventions

TypeNameDescription
DRUGLatanoprost (0.005%)Participants take the eye drop daily for less than one month

Timeline

Start date
2026-07-01
Primary completion
2028-03-01
Completion
2028-03-31
First posted
2026-02-23
Last updated
2026-04-08

Source: ClinicalTrials.gov record NCT07425535. Inclusion in this directory is not an endorsement.