CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,830 enrolled
Drug / intervention
Bimatoprost Ophthalmic Solutiondrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01853085
NCT01853085N/ACompleted

A Study of Patients With Primary Open Angle Glaucoma or Ocular Hypertension Switched to Lumigan® UD Monotherapy for Medical Reasons

Allergan·observational·Posted May 14, 2013·Updated Apr 19, 2019

In Brief

An observational study evaluating Bimatoprost Ophthalmic Solution for Glaucoma, Primary Open Angle and Ocular Hypertension. Completed, enrolled 1,830 participants across 1 site.

Detailed Summary

The study will evaluate patients diagnosed with primary open angle glaucoma or ocular hypertension who are switched to Lumigan® UD monotherapy for medical reasons in accordance with physician standard clinical practice. All treatment decisions lie with the physician.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesGermany
Collaborators--

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedMay 14, 2013
Enrollment StartApr 1, 2013
Primary CompletionMar 1, 2014
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 13.1 years ago

Interventions

Bimatoprost Ophthalmic Solutiondrug

Patients with primary open angle glaucoma (POAG) or ocular hypertension (OHT) treated with Lumigan® UD (bimatoprost ophthalmic solution) administered in accordance with physician standard practice for up to 12 weeks.