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Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes Clinical Trials Data presented on Clinical Trials Search is not meant to be a substitute for qualified health advice, visits or treatment with a real mD. We are not doctors. Always consult your doctor about Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes conditions. Clinical Trials Search.org is a site devoted to listing clinical research studies in human subjects. Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes Clinical research trials and Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes healthcare trials happen in many of places across the United States. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials generally assess the effectivity of new drugs. The purpose of the studies / projects is to solve particular human medical questions. Clinical trials are a popular way for doctors, government agencies, and private sector companies to discover cures for all varieties of conditions, such as Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes. Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes Clinical Trials and other clinical trials allow volunteers to have health treatment alternatives before they are available to the masses. Some times the human subjects obtain treatment for without cost, and sometimes they are compensated for their time. Occasionally there is a cost for a Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes clinical trial. Test subjects oftentimes receive the most effective healthcare possible for their Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes condition. Dangers are a reality, however, and may include extra or frequent physician visits, healthcare dangers (possibly life-jeopardising), and/or the treatment being uneffective. Trials are federally governed with rigorous guidelines to protect clinical trials patients.

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Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes



Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes

For Condition: Open-Angle Glaucoma,Ocular Hypertension
Status: Recruiting
Sponsor(s): Alcon Research ,
Synopsis: To monitor iris pigmentation changes over a five year period in subjects with open-angle glaucoma or ocular hypertension who have experienced an iris pigmentation change while dosing with TRAVATAN.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety Study
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: Subjects of any race and of either sex diagnosed with open-angle glaucoma (with or without pseudoexfoliation or pigment dispersion component) or ocular hypertension who have experienced an iris pigmentation change while dosing with TRAVATAN and who are currently using TRAVATAN
Total Enrollment: 

Location and Contact Information:

Alcon Call Center For Locations *Recruiting*
Multiple Cities & Multiple States,  Texas, 
United States
Recruiting  


Additional Information:
Study ID Numbers:
  C-01-79;  C-01-79
Study Start Date: 
Record last reviewed: June 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00047554

Other Open-Angle Glaucoma Studies:
1. Phase II safety and efficacy study to evaluate a glaucoma therapy in open-angle glaucoma or ocular hypertension patients

2. A safety and efficacy study of Travoprost 0.004% compared to Latanoprost 0.005% in patients with chronic angle-closure glaucoma

3. Pigment Dispersion Syndrome With and Without Glaucoma

4. Abnormalities of the Eye's Anterior Chamber, Iris, Cornea and Lens

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

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Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes

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