NCT04401982RecruitingPhase 4
Measuring the Effects of Netarsudil, Latanoprost, and Combination Therapy on Episcleral and Retinal Blood Flow in Ocular Hypertension and Glaucoma Suspects
Measuring the Effects of Netarsudil, Latanoprost, and Combination Therapy on Episcleral and Retinal Blood Flow in Ocular Hypertension and Glaucoma Suspects Using Erythrocyte Mediated Angiography In Vivo
Source: ClinicalTrials.gov · Last updated 2 Jul 2026
Brief summary (registry, in English)
The goal of this clinical trial is to compare participants treated with latanoprost to those treated with Rocklatan (netarsudil/latanoprost) to determine whether the addition of netarsudil results in greater improvements in episcleral venous blood flow in adults with glaucoma or ocular hypertension. Episcleral venous blood flow will be measured using erythrocyte-mediated angiography (EMA) and laser speckle contrast imaging (LSCI). The main questions this study aims to answer are: * Does Rocklatan produce greater increases in episcleral venous blood flow than latanoprost alone? * Can EMA and LSCI reliably detect changes in episcleral venous blood flow following treatment with these medications? Participants will: * Be randomized to receive either latanoprost or Rocklatan * Undergo imaging of the episcleral veins using EMA and LSCI before, during, and after treatment, and * Complete study visits that include standard ophthalmic examinations and intraocular pressure measurements. Hypothesis: The investigators hypothesize that latanoprost, which primarily increases uveoscleral outflow, will not significantly affect the distal episcleral circulation. In contrast, Rocklatan, through its netarsudil component, is expected to produce measurable increases in episcleral venous flow.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- First submitted
- 20 May 2020
- Start date
- 2 Jul 2026
- Primary completion date
- 17 Mar 2027
- Lead sponsor
- University of Maryland, Baltimore
- Diseases
- Glaucoma, High blood pressure
- NCT number
- NCT04401982
What you commit to
- Study type: Interventional · Phase 4
- Planned participants: 50
- From 2 Jul 2026 to the primary completion date, 17 Mar 2027
- 4 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- 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.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Physicians Inc. Coordinator of this site? Confirm its status | Baltimore | United States | Recruiting |
| University of Maryland Medical Center Coordinator of this site? Confirm its status | Baltimore | United States | Recruiting |
| UM Faculty Physicians, Inc. | 5900 Waterloo Crossing Coordinator of this site? Confirm its status | Columbia | United States | Recruiting |
| Maryland Eye Consultants and Surgeons Coordinator of this site? Confirm its status | Silver Spring | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.