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Internet-based, Naturalistic Evaluation of Tolerability and Individual Patient Target Pressures With Bimatoprost 0.03% in Glaucoma

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Allergan

Status

Completed

Conditions

Glaucoma, Open-Angle

Study type

Observational

Funder types

Industry

Identifiers

NCT00487214
MEDNET2001

Details and patient eligibility

About

The purpose of this study is to evaluate the range of target IOPs set for glaucoma patients starting monotherapy with bimatoprost and to evaluate patient and physician satisfaction with bimatoprost in "real-world" settings

Enrollment

361 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patients with either open-angle glaucoma or ocular hypertension were eligible if they needed bilateral IOP reduction beyond what was achieved with their current medication, or if they were intolerant of other IOP-lowering medications.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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