|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | Alcon Research |
|---|---|
| Information provided by: | Alcon Research |
| ClinicalTrials.gov Identifier: | NCT00047528 |
Purpose
To compare intraocular pressure lowering effectiveness of a combination drug vs. two individual drugs dosed alone.
| Condition | Intervention | Phase |
|---|---|---|
|
Open-Angle Glaucoma Ocular Hypertension |
Drug: Alcon Investigational Agent |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | Phase III Safety and Efficacy Study to Evaluate Combination IOP Lowering Therapy in Open Angle Glaucoma and Ocular Hypertensive Patients (C-02-41). |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Adult subjects of either sex and any race with open-angle glaucoma or ocular hypertension; visual acuity of 20/80 to 20/400 or better (Snellen equivalent) or logMAR visual acuity not worse than 0.6. Clinically relevant ophthalmic or systemic conditions may be excluded.
Contacts and Locations
More Information
| Study ID Numbers: | C-02-41, C-02-41 |
| Study First Received: | October 8, 2002 |
| Last Updated: | August 4, 2008 |
| ClinicalTrials.gov Identifier: | NCT00047528 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
open-angle glaucoma ocular hypertension POAG |
|
Glaucoma Eye Diseases Glaucoma, Open-Angle Vascular Diseases |
Cardiovascular Diseases Ocular Hypertension Hypertension |