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Completed Phase 2 Interventional Results available

Bimatoprost Ocular Insert Compared to Topical Timolol Solution in Patients With Glaucoma or Ocular Hypertension

ClinicalTrials.gov ID: NCT01915940

Public ClinicalTrials.gov record NCT01915940. 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 24, 2026, 6:44 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 2, Multicenter, Randomized, Subject- and Examiner-masked, Controlled Clinical Trial Designed to Evaluate the Safety and Effectiveness of the Bimatoprost Ocular Insert as Compared to Topical Timolol Solution (0.5%) in Patients With Glaucoma or Ocular Hypertension.

Study identification

NCT ID
NCT01915940
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
ForSight Vision5, Inc.
Industry
Enrollment
169 participants

Conditions and interventions

Interventions

  • Bimatoprost Drug
  • Timolol 0.5% Drug
  • Placebo Eye Drops Drug
  • Placebo Ocular Insert Device

Drug · Device

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
Oct 22, 2013
Primary completion
Sep 29, 2014
Completion
Nov 13, 2014
Last update posted
Apr 19, 2018

2013 – 2014

United States locations

U.S. sites
10
U.S. states
6
U.S. cities
10
Facility City State ZIP Site status
Sall Medical Research Center Artesia California 90701
Scripps Clinic Torrey Pines La Jolla California 92037
Eye Research Foundation Newport Beach California 92663
UC Davis Dept of Ophthalmology & Vision Science Sacramento California 95817
Coastal Research Associates Atlanta Georgia 30076
Clayton Eye Center Morrow Georgia 30260
Ophthalmology Consultants St Louis Missouri 63131
UNC Kittner Eye Center Chapel Hill North Carolina 27517
Apex Eye Madeira Ohio 45243
Ophthalmology Associates PC Fort Worth Texas 76102

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 NCT01915940, 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 Apr 19, 2018 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01915940 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →