A Safety Study of Bimatoprost in Patients With Glaucoma or Ocular Hypertension
Completed · Phase 3
Conditions studied: Glaucoma, Ocular Hypertension
In brief
This safety study will evaluate bimatoprost 0.01% and 0.03% in patients with glaucoma or ocular hypertension (OHT).
Key facts
- Study ID
- NCT01830140
- Run by
- Allergan
- People needed
- 466
- Starts
- 2013-07-01
- Expected to finish
- 2014-05-01
- Last updated by the study team
- 2015-05-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of glaucoma or ocular hypertension
You may not qualify if…
- Active ocular disease other than glaucoma or ocular hypertension
- Require chronic use of ocular medications other than the study medication during the study (intermittent use of artificial tear solution will be permitted)
Where it is running
- Study site — Artesia, California, United States
- Study site — El Paso, Texas, United States
Full record on ClinicalTrials.gov
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