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Phase 3 study comparing IOP lowering in OAG or OH in Japanese subjects C-01-98



Phase 3 study comparing IOP lowering in OAG or OH in Japanese subjects C-01-98

For Condition: Open-Angle Glaucoma,Ocular Hypertension
Status: No longer recruiting
Sponsor(s): Alcon Research ,
Synopsis: The purpose of this study is to evaluate safety and efficacy of two different IOP lowering medications after twelve months of treatment in Japanese subjects.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: Adults of Japanese Ethnicity
Total Enrollment: 

Location and Contact Information:


Additional Information:
Study ID Numbers:
  C-01-98;  C-01-98
Study Start Date: 
Record last reviewed: September 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00047593

Other Ocular Hypertension Studies:
1. Safety and Efficacy Study of BETAXON 0.5% and AZOPT 1.0% in Pediatric Patients with Glaucoma or Ocular Hypertension

2. Phase 3 study comparing IOP lowering in OAG or OH in Japanese subjects C-01-98

3. Phase 3 study to evaluate IOP lowering therapy in open angle glaucoma and ocular hypertension C-01-70

4. A safety and efficacy study of Travoprost 0.004% compared to Latanoprost 0.005% in patients with open-angle glaucoma(OAG) or ocular hypertension(OHT)

5. Pigment Dispersion Syndrome With and Without Glaucoma

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Phase 3 study comparing IOP lowering in OAG or OH in Japanese subjects C-01-98

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