NCT00051194

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
Completed

Started Sep 2002

Shorter than P25 for phase_2

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2002

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

January 3, 2003

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 7, 2003

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2003

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2003

Completed
Last Updated

April 16, 2012

Status Verified

March 1, 2006

Enrollment Period

10 months

First QC Date

January 3, 2003

Last Update Submit

April 12, 2012

Conditions

Glaucoma, Open-angleOcular Hypertension

Keywords

GlaucomaPOAGOAGOHT

Interventions

Combination IOP Lowering TherapyDRUG

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Adult patients of any race and either sex with open angle glaucoma or ocular hypertension.

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

Study Sites (1)

Europe

Fort Worth, Texas, 76134, United States

Location

MeSH Terms

Conditions

Glaucoma, Open-AngleOcular HypertensionGlaucoma

Condition Hierarchy (Ancestors)

Eye Diseases

Study Officials

  • Alcon Investigators

    Alcon Research

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
DOUBLE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 3, 2003

First Posted

January 7, 2003

Study Start

September 1, 2002

Primary Completion

July 1, 2003

Study Completion

July 1, 2003

Last Updated

April 16, 2012

Record last verified: 2006-03

Locations

US(1)