Distribution of Risk Factors in Ocular Hypertension and Open-Angle Glaucoma Patients in Canada

Overview

This descriptive, non-interventional study will collect information on the presence of risk factors in newly diagnosed ocular hypertension and open-angle glaucoma patients in Canada.

Full Title of Study: “Distribution of Risk Factors Amongst Ocular Hypertension and Open-Angle Glaucoma Patients in Canada”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: April 2009

Interventions

  • Other: There is no intervention in this study.
    • This study is collecting information on the presence of risk factors in new diagnosed OH and OAG patients in Canada.

Arms, Groups and Cohorts

  • There is no intervention in this study
    • This study is collecting information on the presence of risk factors in new diagnosed OH and OAG patients in Canada.

Clinical Trial Outcome Measures

Primary Measures

  • To describe the presence and distribution of risk factors in subjects diagnosed with OH or OAG stratified according to geographic distribution in a Canadian population in the ophthalmologist practice.
    • Time Frame: duration of study

Secondary Measures

  • To describe the severity of disease at the time of diagnosis and to determine if there is a correlation between risk factors, or number of risk factors, and the severity of disease at presentation.
    • Time Frame: duration of study

Participating in This Clinical Trial

Inclusion Criteria

  • Subjects diagnosed at study visit or within 3 months of visit with OH – OAG (to include POAG, NTG, pigmentary and pseudoexfoliation glaucoma) Exclusion Criteria:

  • No prior treatment for OH or OAG – No prior ocular surgery or history of ocular trauma

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Pfizer’s Upjohn has merged with Mylan to form Viatris Inc.
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Pfizer CT.gov Call Center, Study Director, Pfizer

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