Glaucoma, Open-Angle
Conditions
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.
Interventions
OTHERStandard of Care
Patients with glaucoma treated with standard of care at the discretion of the physician. There is no specific treatment required for this study.
Sponsors
Allergan
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* Glaucoma in one or both eyes
Exclusion criteria
* Participation in a glaucoma therapeutic clinical trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change from Baseline in Visual Field | Baseline, 24 Months |
Secondary
| Measure | Time frame |
|---|---|
| Change from Baseline in Intraocular Pressure (IOP) | Baseline, 24 Months |
Countries
Spain
Outcome results
None listed