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NCT06883123 · ClinicalTrials.gov registry record · Phase 4

Efficacy of Simbrinza and Rocklatan vs Cosopt and Latanoprost

A Phase 4 study of Open Angle Glaucoma, sponsored by Prairie Eye Center.

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

NCT06883123 is a Phase 4 study of Open Angle Glaucoma that is actively recruiting participants, run by Prairie Eye Center. The registered enrollment target is 70 participants, below the 332-participant average among 28 other Open Angle Glaucoma trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06883123, a Phase 4 study of Open Angle Glaucoma, is actively recruiting participants, sponsored by Prairie Eye Center.

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

Study Summary

A randomized, multi-site, parallel-group, prospective study of patients who are adults with a diagnosis of mild to moderate open-angle glaucoma (OAG), currently on an on-label use of combination topical medication of Cosopt and Latanoprost for a minimum of 1 month.

Conditions Studied

Interventions

  • DRUG Latanoprost 0.005% Ophthalmic Solution
  • DRUG Simbrinza 0.2%-1% Ophthalmic Suspension
  • DRUG Rocklatan 0.02%-0.005% Ophthalmic Solution
  • DRUG Cosopt PF 2%-0.5% Ophthalmic Solution

Study Locations (1)

Illinois

  • Prairie Eye Center - Springfield

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2025-05-14
Est. Completion 2026-04-01
Phase Phase 4

Sponsor

Prairie Eye Center

1 total trials

What the Registry Record Tells You About NCT06883123

The ClinicalTrials.gov registry entry for NCT06883123 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 332-participant average among 28 other Open Angle Glaucoma trials with a reported enrollment target (79% lower). The listed sponsor is Prairie Eye Center, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Open Angle Glaucoma appearing as the primary indexed condition, and to 4 interventions - of which Latanoprost 0.005% Ophthalmic Solution is the first listed.

NCT06883123 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT06883123 about?

NCT06883123 is a clinical study titled "Efficacy of Simbrinza and Rocklatan vs Cosopt and Latanoprost". A randomized, multi-site, parallel-group, prospective study of patients who are adults with a diagnosis of mild to moderate open-angle glaucoma (OAG), currently on an on-label use of combination topical medication of Cosopt and Latanoprost for a minimum of 1 month.

What is the current status of trial NCT06883123?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 70 participants. The study started on 2025-05-14. Estimated completion is 2026-04-01.

What conditions does trial NCT06883123 study?

This clinical trial studies the following conditions: Open Angle Glaucoma.

What interventions are being tested in trial NCT06883123?

The interventions under investigation include: Latanoprost 0.005% Ophthalmic Solution (DRUG), Simbrinza 0.2%-1% Ophthalmic Suspension (DRUG), Rocklatan 0.02%-0.005% Ophthalmic Solution (DRUG), Cosopt PF 2%-0.5% Ophthalmic Solution (DRUG).

Who is sponsoring clinical trial NCT06883123?

This trial is sponsored by Prairie Eye Center, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06883123 being conducted?

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

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

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