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A Study of Lumigan® in Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT)

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Allergan

Status

Completed

Conditions

Ocular Hypertension
Glaucoma, Open-Angle

Treatments

Drug: bimatoprost 0.01%

Study type

Observational

Funder types

Industry

Identifiers

NCT01632423
MAF/AGN/OPH/GLA/025

Details and patient eligibility

About

This is an observational study of Lumigan® 0.01% (bimatoprost) treatment in clinical practice for patients with Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT).

Enrollment

10,337 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with primary open angle glaucoma or ocular hypertension
  • Prescribed Lumigan®

Exclusion criteria

  • None

Trial design

10,337 participants in 1 patient group

POAG or OHT
Description:
Patients with POAG or OHT prescribed Lumigan® (bimatoprost 0.01%) treatment in a dose determined by the physician prior to study entry
Treatment:
Drug: bimatoprost 0.01%

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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