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A 6-week safety & efficacy study of combination intraocular pressure-lowering therapy in patients with open-angle glaucoma or ocular hypertension



A 6-week safety & efficacy study of combination intraocular pressure-lowering therapy in patients with open-angle glaucoma or ocular hypertension

For Condition: Glaucoma, Open-Angle,Ocular Hypertension
Status: Recruiting
Sponsor(s): Alcon Research ,
Synopsis: To compare the intraocular pressure(IOP)-lowering efficacy of morning or evening instillations of a combination IOP-lowering therapy in patients with open-angle glaucoma or ocular hypertension.
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: Adult patients of any race and either sex with open angle glaucoma or ocular hypertension.
Total Enrollment: 

Location and Contact Information:

Europe *Recruiting*
,  , 

Recruiting  


Additional Information:
Study ID Numbers:
  C-02-03; 
Study Start Date: 
Record last reviewed: January 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00051194

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4. Pigment Dispersion Syndrome With and Without Glaucoma

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