A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paediatric Patients With Glaucoma



Status:Terminated
Conditions:Ocular
Therapuetic Areas:Ophthalmology
Healthy:No
Age Range:Any - 17
Updated:4/21/2016
Start Date:September 2011
End Date:October 2014

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The purpose of this study is to assess the safety and efficacy of a new formulation of
bimatoprost ophthalmic solution compared to timolol ophthalmic solution in the treatment of
paediatric patients with glaucoma.


Inclusion Criteria:

- Diagnosis of congenital, juvenile glaucoma

- Requires treatment with IOP-lowering medication in one or both eyes

Exclusion Criteria:

- Surgical intervention is indicated or planned to lower IOP

- Abnormally low body weight (below 5th percentile)

- Any active eye infection or disease

- Anticipated use of contact lenses during the study

- Topical ocular steroid use within 2 months

- History of ocular trauma in either eye

- Required chronic use of ocular medications (other than study medication) during the
study (intermittent use of artificial tears permitted)
We found this trial at
2
sites
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mi
from
Louisville, KY
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mi
from
Amiens,
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