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N/A N=4,812

A Study of Intraocular Pressure (IOP) Reduction in Newly Diagnosed Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT)

Glaucoma, Open-Angle · Ocular Hypertension

Enrolled (actual)
4,812
Serious AEs
0.0%
Results posted
Sep 2012
Primary outcome: Primary: Percentage of Patients With a Reduction in Intraocular Pressure (IOP) ≥ 5mmHg From Baseline — 75.9 Millimeters of Mercury (mmHg)

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Standard of Care (Other)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Allergan
Primary completion
Jul 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Patients With a Reduction in Intraocular Pressure (IOP) ≥ 5mmHg From Baseline
75.9
SECONDARY
Percentage of Patients With an IOP Reduction ≥10% From Baseline
91.0
SECONDARY
Percentage of Patients With an IOP Reduction ≥20% From Baseline
70.8

Summary

This is an observational study and will evaluate IOP reduction in newly diagnosed patients with POAG or OHT. All care (including treatment and diagnostic procedures) provided is at the discretion of the participating physicians according to their clinical judgment and the local standard of medical care.

Eligibility Criteria

Inclusion Criteria

  • Newly diagnosed with primary open angle glaucoma or ocular hypertension

Exclusion Criteria

  • None
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01628614). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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