Eye drops aim to boost blood flow in glaucoma suspects
NCT ID NCT04401982
First seen Jul 02, 2026 · Last updated Jul 02, 2026
Summary
This study compares two eye drop treatments—latanoprost alone versus a combination of netarsudil and latanoprost (Rocklatan)—to see if the combination improves blood flow in the veins around the eye. Researchers will use special imaging techniques to measure blood flow in adults with ocular hypertension or suspected glaucoma. The goal is to understand whether adding netarsudil can increase blood flow beyond what latanoprost does alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Rocklatan (netarsudil/latanoprost) and latanoprost
- What this could lead to
- If successful, this could show that netarsudil improves eye blood flow, potentially leading to better treatments for glaucoma.
- What could go wrong
- This is a small, early-phase study focused on measuring blood flow, not on long-term outcomes. The results may not translate to better vision or disease control.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion: * Patients are at least 18 years of age. * Patients must have ocular hypertension or be a glaucoma suspect. * Patient must not have used any IOP-lowering medication (topical or systemic) within the past 6 months * Patients must have open angles on gonioscopy. * All patients will have at least one recorded visual field examination within 6 months of enrollment in the study. Visual fields will be assessed using the Hodapp-Andersen-Parish criteria. Exclusion: * Participation in other investigational studies, unless such participation does not involve the administration of any drugs or agents that could impact the results of this study or have an effect on episcleral flow, as determined by the Investigator. * Prior intraocular surgery other than uncomplicated cataract surgery. * Allergy or history of adverse reaction to ICG, shellfish, or Iodine. * Significant liver disease or uremia. * Secondary glaucoma including exfoliation glaucoma, pigmentary glaucoma, or history of acute angle closure. * Moderate or severe visual field deficits as per Hodapp-Anderson-Parish criteria. * Any condition precluding imaging including reliable visual fields, disc photography, or use of study treatments including media opacity or tilted optic disk * Pregnant or nursing patients.
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
Locations
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Maryland Eye Consultants and Surgeons
RECRUITINGSilver Spring, Maryland, 20902, United States
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UM Faculty Physicians, Inc. | 5900 Waterloo Crossing
RECRUITINGColumbia, Maryland, 21045, United States
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University Physicians Inc.
RECRUITINGBaltimore, Maryland, 21201, United States
Contact Email: •••••@•••••
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University of Maryland Medical Center
RECRUITINGBaltimore, Maryland, 21201, United States
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Other studies related to the condition(s) this trial covers.
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- Could a single eye implant replace years of glaucoma drops?
- Which eye implant best tames glaucoma? a head-to-head trial aims to find out.