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Prednisolone Ophthalmic |
AK-Pred; Econopred; Econopred Plus; Inflamase Forte; Inflamase Mild; Pred Forte; Pred Mild |
Clinical Trial: Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes
This study is currently recruiting patients.
|
Purpose
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.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Open-Angle Glaucoma Ocular Hypertension | Drug: TRAVATAN (travoprost ophthalmic solution) 0.004% | Phase IV |
MedlinePlus related topics: Eye Diseases; Glaucoma
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety Study
Official Title: A Phase IV safety study of TRAVATAN 0.004% in subjects with TRAVATAN induced iris pigmentation changes C-01-79.
Eligibility
Genders Eligible for Study: Both
Criteria
Location and Contact Information
Texas
Alcon Call Center For Locations, Multiple Cities & Multiple States, Texas, United States; Recruiting
More Information
Record last reviewed: June 2003
Last Updated: October 13, 2004
Record first received: October 8, 2002
ClinicalTrials.gov Identifier: NCT00047554
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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