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NCT00051194 Clinical Trial

A 6-week Safety & Efficacy Study of Combination Intraocular Pressure-lowering Therapy in Patients With Open-angle Glaucoma or Ocular Hypertension

Ocular Hypertension Clinical Trial

Official title:
A 6-week Safety and Efficacy Study of Combination IOP-lowering Therapy in Patients With Open-angle Glaucoma or Ocular Hypertension.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00051194
Other study ID # C-02-03
Secondary ID
Status Completed
Phase Phase 2
First received January 3, 2003
Last updated April 12, 2012
Start date September 2002
Est. completion date July 2003

Study information
Verified date March 2006
Source Alcon Research
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date July 2003
Est. primary completion date July 2003
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Adult patients of any race and either sex with open angle glaucoma or ocular hypertension.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Combination IOP Lowering Therapy

Locations
Country Name City State
United States Europe Fort Worth Texas

Sponsors (1)
Lead Sponsor Collaborator
Alcon Research

Country where clinical trial is conducted

United States, 

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