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NCT06865144 · ClinicalTrials.gov registry record · Phase 4

Effect of Rhopressa on Intraocular Pressure (IOP) in Patients With Primary Open-Angle Glaucoma or Ocular Hypertension Post-SLT

A Phase 4 study of Primary Open Angle Glaucoma or Ocular Hypertension, sponsored by East Coast Institute for Research.

Recruiting
Registry status
Phase 4
Development phase
70
Enrollment target
1
Study location

NCT06865144: Recruiting Phase 4 study of Primary Open Angle Glaucoma or Ocular Hypertension, sponsored by East Coast Institute for Research.

NCT06865144 is a Phase 4 study of Primary Open Angle Glaucoma or Ocular Hypertension that is actively recruiting participants, run by East Coast Institute for Research. The registered enrollment target is 70 participants, above the 41-participant average among 3 other Primary Open Angle Glaucoma or Ocular Hypertension trials with a reported enrollment target (71% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06865144, a Phase 4 study of Primary Open Angle Glaucoma or Ocular Hypertension, is actively recruiting participants, sponsored by East Coast Institute for Research.

RECRUITING
Registry status
Phase 4
Development phase
70 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to collect data about how Rhopressa affects IOP in patients who have had an SLT procedure in both eyes.

Primary Outcome

Between-group difference in change in mean diurnal IOP

Interventions

  • DRUG Netarsudil ophthalmic solution 0.02%
  • DRUG Artificial tears

Study Locations (1)

Florida

  • East Coast Institute for Research at Florida Eye Specialists - Jacksonville

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2025-06-27
Est. Completion 2026-04-01
Phase Phase 4

What NCT06865144 shows while recruiting

NCT06865144 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, above the 41-participant average among 3 other Primary Open Angle Glaucoma or Ocular Hypertension trials with a reported enrollment target (71% higher).

The record links to 1 condition, with Primary Open Angle Glaucoma or Ocular Hypertension appearing as the primary indexed condition, and to 2 interventions - of which Netarsudil ophthalmic solution 0.02% is the first listed.

NCT06865144 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT06865144 about?

NCT06865144 is a clinical study titled "Effect of Rhopressa on Intraocular Pressure (IOP) in Patients With Primary Open-Angle Glaucoma or Ocular Hypertension Post-SLT". The purpose of this study is to collect data about how Rhopressa affects IOP in patients who have had an SLT procedure in both eyes.

What is the current status of trial NCT06865144?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 70 participants. The study started on 2025-06-27. Estimated completion is 2026-04-01.

What conditions does trial NCT06865144 study?

This clinical trial studies the following conditions: Primary Open Angle Glaucoma or Ocular Hypertension.

What interventions are being tested in trial NCT06865144?

The interventions under investigation include: Netarsudil ophthalmic solution 0.02% (DRUG), Artificial tears (DRUG).

Who is sponsoring clinical trial NCT06865144?

This trial is sponsored by East Coast Institute for Research, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06865144 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06865144, the US trial registry maintained by the National Library of Medicine. NCT06865144 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.