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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.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Wiesloch, Baden-Wurttemberg, Germany
Start Date
April 1, 2013
Primary Completion Date
March 1, 2014
Completion Date
March 1, 2014
Last Updated
April 19, 2019
1,830
ACTUAL participants
Bimatoprost Ophthalmic Solution
DRUG
Lead Sponsor
Allergan
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT03675412