NCT01629407
Completed
Not Applicable
A Study of the Rate of Progression of Glaucoma During a Follow-up Period of Two Years
ConditionsGlaucoma, Open-Angle
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Glaucoma, Open-Angle
- Sponsor
- Allergan
- Enrollment
- 315
- Primary Endpoint
- Change from Baseline in Visual Field
- Status
- Completed
- Last Updated
- 12 years ago
Overview
Brief Summary
This is an epidemiological, non-interventional, prospective study to collect data on glaucoma progression in a routine setting. Patients may receive treatment at the discretion of their physician per local standard of care.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Glaucoma in one or both eyes
Exclusion Criteria
- •Participation in a glaucoma therapeutic clinical trial
Outcomes
Primary Outcomes
Change from Baseline in Visual Field
Time Frame: Baseline, 24 Months
Secondary Outcomes
- Change from Baseline in Intraocular Pressure (IOP)(Baseline, 24 Months)
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