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Memantine in Patients With Chronic Glaucoma

Primary Purpose

Open-Angle Glaucoma

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
memantine
Sponsored by
Allergan
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Open-Angle Glaucoma

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Glaucoma damage on examination of visual field and optic disc Good visual acuity (with glasses if needed)

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Progression of glaucoma

    Secondary Outcome Measures

    Full Information

    First Posted
    August 31, 2005
    Last Updated
    November 3, 2010
    Sponsor
    Allergan
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00141882
    Brief Title
    Memantine in Patients With Chronic Glaucoma
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2010
    Overall Recruitment Status
    Completed
    Study Start Date
    March 1999 (undefined)
    Primary Completion Date
    January 2006 (Actual)
    Study Completion Date
    August 2006 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Allergan

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Randomized double-masked clinical trial of memantine in patients with glaucoma

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Open-Angle Glaucoma

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    Double
    Allocation
    Randomized
    Enrollment
    1119 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    memantine
    Primary Outcome Measure Information:
    Title
    Progression of glaucoma

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Glaucoma damage on examination of visual field and optic disc Good visual acuity (with glasses if needed)

    12. IPD Sharing Statement

    Learn more about this trial

    Memantine in Patients With Chronic Glaucoma

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