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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01629407
Other study ID # MAF/AGN/OPH/GLA/015
Secondary ID
Status Completed
Phase N/A
First received June 25, 2012
Last updated June 19, 2013
Start date June 2009
Est. completion date May 2013

Study information

Verified date June 2013
Source Allergan
Contact n/a
Is FDA regulated No
Health authority Spain: Ethics Committee
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 315
Est. completion date May 2013
Est. primary completion date May 2013
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Glaucoma in one or both eyes

Exclusion Criteria:

- Participation in a glaucoma therapeutic clinical trial

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Standard 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.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Allergan

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline in Visual Field Baseline, 24 Months No
Secondary Change from Baseline in Intraocular Pressure (IOP) Baseline, 24 Months No
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