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Phase 4 Study Comparing IOP Lowering in OAG or OH in Caucasian or Japanese Subjects C-02-32

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Alcon

Status and phase

Terminated
Phase 4

Conditions

Open-angle Glaucoma
Ocular Hypertension

Treatments

Drug: IOP Lowering Medications

Study type

Interventional

Funder types

Industry

Identifiers

NCT00047606
C-02-32

Details and patient eligibility

About

The purpose of this study is to evaluate safety and efficacy of two different IOP lowering medications after six weeks of treatment in Caucasian and Japanese subjects.

Enrollment

84 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Adults of Caucasian and Japanese Ethnicity

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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