Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04401982 · ClinicalTrials.gov registry record · Phase 4

Measuring the Effects of Netarsudil, Latanoprost, and Combination Therapy on Episcleral and Retinal Blood Flow in Ocular Hypertension and Glaucoma Suspects

A Phase 4 study, sponsored by University of Maryland, Baltimore.

Recruiting
Registry status
Phase 4
Development phase
50
Enrollment target

NCT04401982 is a Phase 4 study that is actively recruiting participants, run by University of Maryland, Baltimore. The registered enrollment target is 50 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04401982, a Phase 4 study, is actively recruiting participants, sponsored by University of Maryland, Baltimore.

RECRUITING
Registry status
Phase 4
Development phase
50 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG Latanoprost (0.005%)
  • DRUG Rocklatan (Netarsudil 0.02%/ latanoprost 0.005)

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2026-07-02
Est. Completion 2027-03-17
Phase Phase 4

Sponsor

University of Maryland, Baltimore

560 total trials

What the Registry Record Tells You About NCT04401982

The ClinicalTrials.gov registry entry for NCT04401982 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Maryland, Baltimore, which has 560 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Latanoprost (0.005%) is the first listed.

NCT04401982 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04401982 about?

NCT04401982 is a clinical study titled "Measuring the Effects of Netarsudil, Latanoprost, and Combination Therapy on Episcleral and Retinal Blood Flow in Ocular Hypertension and Glaucoma Suspects". 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....

What is the current status of trial NCT04401982?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2026-07-02. Estimated completion is 2027-03-17.

What interventions are being tested in trial NCT04401982?

The interventions under investigation include: Latanoprost (0.005%) (DRUG), Rocklatan (Netarsudil 0.02%/ latanoprost 0.005) (DRUG).

Who is sponsoring clinical trial NCT04401982?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.