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Completed Phase 3 Interventional

Evaluation of the Duration of Effect of Bimatoprost SR in Participants With Open-Angle Glaucoma or Ocular Hypertension

ClinicalTrials.gov ID: NCT03850782

Public ClinicalTrials.gov record NCT03850782. 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 Jul 23, 2026, 4:01 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 Phase 3b Study to Evaluate the Duration of Effect of Bimatoprost SR in Participants With Open-Angle Glaucoma or Ocular Hypertension

Study identification

NCT ID
NCT03850782
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AbbVie
Industry
Enrollment
515 participants

Conditions and interventions

Interventions

  • Bimatoprost (SR) Drug

Drug

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
Feb 27, 2019
Primary completion
Aug 7, 2025
Completion
Aug 7, 2025
Last update posted
Aug 18, 2025

2019 – 2025

United States locations

U.S. sites
38
U.S. states
20
U.S. cities
35
Facility City State ZIP Site status
Horizon Eye Specialists & Lasik Centers /ID# 235240 Sun City Arizona 85351
Atlantis Eye Care /ID# 235530 Huntington Beach California 92647
Lakeside Vision Center /ID# 234970 Irvine California 92604
Global Research Foundation /ID# 237350 Los Angeles California 90041-1718
The Eye Research Foundation /ID# 234521 Newport Beach California 92663-3637
Byers Eye Institute Stanford /ID# 235544 Palo Alto California 94303
Foothill Eye Institute /ID# 235640 Pasadena California 91107
Connecticut Eye Consultants P.C. /ID# 234981 Danbury Connecticut 06810
Advanced Research, LLC /ID# 236045 Deerfield Beach Florida 33064-1342
Segal Drug Trials, Inc /ID# 235784 Delray Beach Florida 33484
International Research Center /ID# 238050 Tampa Florida 33603
Thomas Eye Group PC /ID# 235737 Sandy Springs Georgia 30328
Indiana University - Glick Eye Institute /ID# 235886 Indianapolis Indiana 46202
Retina Partners Midwest, PC /ID# 237876 Indianapolis Indiana 46290
Tulane University School of Medicine /ID# 237632 New Orleans Louisiana 70112
Ophthalmic Consultants of Boston /ID# 236534 Boston Massachusetts 02129
Clinical Eye Research of Boston LLC /ID# 234966 Winchester Massachusetts 01890
University of Michigan, Kellogg Eye Center /ID# 236496 Ann Arbor Michigan 48105
Fraser Eye Center /ID# 235790 Fraser Michigan 48026
Silverstein Eye Centers /ID# 237881 Kansas City Missouri 64034
Moyes Eye Centers /ID# 234989 Kansas City Missouri 64154
Alterman Modi & Wolter /ID# 235248 Poughkeepsie New York 12603-2455
The Ohio State University /ID# 236790 Columbus Ohio 43210-1257
AMA Eyes Research Institute /ID# 235542 Marysville Ohio 43040
Dean McGee Eye Institute /ID# 236823 Oklahoma City Oklahoma 73104
Oklahoma Eye Surgeons /ID# 235849 Oklahoma City Oklahoma 73112
Drs Fine Hoffman & Sims LLC /ID# 235918 Eugene Oregon 97401
Ophthalmic Partners, PC /ID# 235741 Bala-Cynwyd Pennsylvania 19004
Scott and Christie and Associates /ID# 234593 Cranberry Township Pennsylvania 16066
Black Hills Regional Eye Institute /ID# 235075 Rapid City South Dakota 57701
Vance Thompson Vision /ID# 235072 Sioux Falls South Dakota 57108
Eye Specialty Group /ID# 235721 Memphis Tennessee 38120
Vanderbilt University Medical Center /ID# 237177 Nashville Tennessee 37232-0011
Advancing Vision Research /ID# 236681 Smyrna Tennessee 37167
ATX Clinical Trials Inc. dba Keystone Research /ID# 235868 Austin Texas 78731
Medical Center Ophthalmology Associates - Keystone Research /ID# 235787 San Antonio Texas 78240
Southern Utah Medical Research /ID# 235602 St. George Utah 84790
Piedmont Eye Center /ID# 234534 Lynchburg Virginia 24502

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 70 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03850782, 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 Aug 18, 2025 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03850782 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →