Phase 3 Study to Evaluate IOP Lowering Therapy in Open Angle Glaucoma and Ocular Hypertension C-01-69

This study has been completed.
Sponsor:
Information provided by:
Alcon Research
ClinicalTrials.gov Identifier:
NCT00047515
First received: October 8, 2002
Last updated: August 4, 2008
Last verified: August 2008

October 8, 2002
August 4, 2008
January 2001
December 2003   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00047515 on ClinicalTrials.gov Archive Site
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Phase 3 Study to Evaluate IOP Lowering Therapy in Open Angle Glaucoma and Ocular Hypertension C-01-69
Phase III Safety and Efficacy Study to Evaluate Combination IOP Lowering Therapy in Open Angle Glaucoma and Ocular Hypertensive Patients C-01-69.

To compare intraocular pressure lowering effectiveness of a combination drug vs. two individual drugs dosed alone.

Not Provided
Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
  • Open-Angle Glaucoma
  • Ocular Hypertension
Drug: Alcon Investigational Agent
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
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December 2003
December 2003   (final data collection date for primary outcome measure)

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.

Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00047515
C-01-69, C-01-69
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Alcon Research
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Alcon Research
August 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP