A 6-Week Safety & Efficacy Study of Combination Intraocular Pressure-Lowering Therapy in Patients With Open-Angle Glaucoma or Ocular Hypertension

This study has been completed.

Sponsored by:	Alcon Research
Information provided by:	Alcon Research
ClinicalTrials.gov Identifier:	NCT00051194

Purpose

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.

Condition	Intervention	Phase
Glaucoma, Open-Angle Ocular Hypertension	Drug: Combination IOP Lowering Therapy	Phase II

Genetics Home Reference related topics: early-onset glaucoma

MedlinePlus related topics: Glaucoma High Blood Pressure

U.S. FDA Resources

Study Type:	Interventional
Study Design:	Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title:	A 6-Week Safety and Efficacy Study of Combination IOP-Lowering Therapy in Patients With Open-Angle Glaucoma or Ocular Hypertension.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Adult patients of any race and either sex with open angle glaucoma or ocular hypertension.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00051194

Locations

United States, Texas
Europe
Fort Worth, Texas, United States

Sponsors and Collaborators

Alcon Research

Investigators

Principal Investigator:

Alcon Investigators

Alcon Research

More Information

Study ID Numbers:	C-02-03
Study First Received:	January 3, 2003
Last Updated:	March 3, 2006
ClinicalTrials.gov Identifier:	NCT00051194
Health Authority:	United States: Food and Drug Administration

Keywords provided by Alcon Research:

Glaucoma
POAG
OAG
OHT

Study placed in the following topic categories:

Glaucoma
Eye Diseases
Glaucoma, Open-Angle

Vascular Diseases
Hypertension
Ocular Hypertension

Additional relevant MeSH terms:

Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 15, 2009