Imaging the Effects of Netarsudil (Rhopressa) on the Trabecular Meshwork in Glaucoma and Ocular Hypertension
Recruiting
Phase 4Interventional Study
GlaucomaOcular Hypertension
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Basic Science
Participants needed
50 (estimated)
Sponsor
Indiana University · Other
Who this trial is looking for
This trial is looking for adults with glaucoma or high eye pressure. Participants will receive either netarsudil eye drops or a placebo and will undergo eye imaging tests over about two weeks.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years or older
I have been diagnosed with ocular hypertension or open-angle glaucoma
I had an eye exam within the past year
I have visual field test results that show glaucoma
My best-corrected vision is 20/100 or better
My eye angle is open as confirmed by tests
My eye pressure is between 18 and 34 mmHg
You may not be able to join if
I am intolerant to netarsudil eye drops
I have corneal scarring or an active eye disease
I cannot tolerate gonioscopy procedures
I am a woman of childbearing potential not using effective contraception
I have a condition that may increase my risk or interfere with the study
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
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This study evaluates the effects of netarsudil (Rhopressa) on the trabecular meshwork in subjects with ocular hypertension or open-angle glaucoma. Participants will be randomized to receive either netarsudil or placebo (artificial tears). High-resolution imaging using adaptive optics gonioscopy, anterior segment optical coherence tomography (AS-OCT), and OCT gonioscopy will be performed at baselin…
This study evaluates the effects of netarsudil (Rhopressa) on the trabecular meshwork in subjects with ocular hypertension or open-angle glaucoma. Participants will be randomized to receive either netarsudil or placebo (artificial tears). High-resolution imaging using adaptive optics gonioscopy, anterior segment optical coherence tomography (AS-OCT), and OCT gonioscopy will be performed at baseline and after approximately 14 days of treatment. The primary objective is to assess changes in trabecular meshwork lamellae spacing, with secondary measures including trabecular meshwork height, width, and Schlemm's canal diameter.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adults aged 18 years or older
* Diagnosis of ocular hypertension or open-angle glaucoma
* Eye examination within the past year
* For glaucoma subjects: structural (optic nerve and/or retinal nerve fiber layer) and functional (visual field) findings consistent with glaucoma
* B…
Inclusion Criteria:
* Adults aged 18 years or older
* Diagnosis of ocular hypertension or open-angle glaucoma
* Eye examination within the past year
* For glaucoma subjects: structural (optic nerve and/or retinal nerve fiber layer) and functional (visual field) findings consistent with glaucoma
* Best-corrected visual acuity of 20/100 or better
* Open anterior chamber angle as confirmed by gonioscopy and anterior segment optical coherence tomography (AS-OCT)
* Intraocular pressure between 18 and 34 mmHg (treatment-naïve or after washout, if applicable)
Exclusion Criteria:
* Known intolerance to netarsudil ophthalmic solution
* Corneal scarring or active corneal disease that would interfere with imaging
* Inability to tolerate gonioscopy procedures
* Females of childbearing potential who are not using effective contraception or are not sterile
* Any condition that, in the opinion of the investigator, would place the subject at increased risk or interfere with study completion
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