Efficacy of Bimatoprost 0.03% in Patients Who Are Low-Responders to Latanoprost
NCT00347841 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL
Last updated 2007-06-01
Summary
To evaluate the IOP-lowering efficacy of bimatoprost 0.03% in patients found to be low-responders to latanoprost therapy.
Conditions
Interventions
- DRUG
-
Bimatoprost 0.03%, Latanoprost
Sponsors & Collaborators
-
Innovative Medical
lead INDUSTRY
Principal Investigators
-
Robert Noecker, MD · UPMC Eye Center
Study Design
- Allocation
- NON_RANDOMIZED
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
Countries
- United States
Study Locations
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