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Completed Phase 4 Interventional Results available

Study of Rhopressa® for the Reduction of Elevated Intraocular Pressure in Patients With Glaucoma or Ocular Hypertension in a Real-world Setting

ClinicalTrials.gov ID: NCT03808688

Public ClinicalTrials.gov record NCT03808688. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 5:45 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Open-label Study of Rhopressa® (Netarsudil Ophthalmic Solution) 0.02% for the Reduction of Elevated Intraocular Pressure in Patients With Glaucoma or Ocular Hypertension in a Real-world Setting

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To evaluate the IOP lowering efficacy of netarsudil ophthalmic solution 0.02% when used as monotherapy or when used concomitantly with other IOP-lowering agents in subjects with elevated IOP due to open angle glaucoma or ocular hypertension in a real-world clinical setting. The study is an open-label design. The patients will receive treatment for 12 weeks.

Study identification

NCT ID
NCT03808688
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Aerie Pharmaceuticals
Industry
Enrollment
261 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 26, 2018
Primary completion
Jul 25, 2019
Completion
Jul 25, 2019
Last update posted
Sep 28, 2020

2018 – 2019

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Atlantis Eyecare Huntington Beach California 92647
Harvard Eye Associates Laguna Hills California 92653
North Bay Eye Associates, Inc Petaluma California 94954
Shettle Eye Research Inc Largo Florida 33773
Center For Sight Sarasota Florida 34238
Coastal Research Associates, LLC Roswell Georgia 30076
Wheaton Eye Clinic, Ltd Wheaton Illinois 60187
Stiles Eyecare Excellence and Glaucoma Institute, PA Overland Park Kansas 66213
Gaddie Eye Centers, LLC Louisville Kentucky 40241
Glaucoma Consultants Baltimore Maryland 21204
Tekwani Vision Center St Louis Missouri 63128
Mark J. Weiss, M.D., Inc. Tulsa Oklahoma 74104
Scott & Christie and Associates, PC Cranberry Township Pennsylvania 16066
Valley Eye Professionals, LLC Huntingdon Valley Pennsylvania 19006
Carolina Cataract & Laser Center Ladson South Carolina 29456
Total Eye Care, PA Memphis Tennessee 38119
VRF Eye Specialty Group Memphis Tennessee 38120
Advancing Vision Research Nashville Tennessee 37204
Keystone Research Austin Texas 78731
Cataract & Glaucoma Center El Paso Texas 79902
Houston Eye Associates Houston Texas 77025
The Eye Centers of Racine and Kenosha Racine Wisconsin 53405

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03808688, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 28, 2020 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03808688 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →