Long-Term Non-Interventional Study (NIS) To Investigate The Safety And Effectiveness Of MACUGEN In Patients With Neovascular Age-Related Macular Degeneration Under Conditions Of Routine Clinical Practice

NCT ID: NCT00787319

Last Updated: 2018-12-06

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

108 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-01-31

Study Completion Date

2012-06-30

Brief Summary

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To define what procedures were used for the diagnosis and monitoring of the treatment age-related macular degeneration (AMD). What is the effect of the Macugen, compliance with Macugen treatment, safety profile of Macugen, final physician assessment of treatment with Macugen.

Detailed Description

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no sampling

Conditions

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Age-related Macular Degeneration

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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AMD

no intervention

Intervention Type OTHER

Outpatients with age-related macular degeneration (AMD)

Interventions

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no intervention

Outpatients with age-related macular degeneration (AMD)

Intervention Type OTHER

Other Intervention Names

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observation only

Eligibility Criteria

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Inclusion Criteria

* age over 18 years old
* patients with neovascular age-related macular degeneration
* enrollment to study is fully on physician decision in compliance with current SPC

Exclusion Criteria

* Patient who did not meet indication according to SPC Macugen.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

Brno, , Czechia

Site Status

Pfizer Investigational Site

Brno, , Czechia

Site Status

Pfizer Investigational Site

Olomouc, , Czechia

Site Status

Pfizer Investigational Site

Olomouc, , Czechia

Site Status

Pfizer Investigational Site

Ostrava - Poruba, , Czechia

Site Status

Pfizer Investigational Site

Pilsen, , Czechia

Site Status

Pfizer Investigational Site

Prague, , Czechia

Site Status

Pfizer Investigational Site

Prague, , Czechia

Site Status

Pfizer Investigational Site

Prague, , Czechia

Site Status

Pfizer Investigational Site

Prague, , Czechia

Site Status

Pfizer Investigational Site

Ústí nad Labem, , Czechia

Site Status

Countries

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Czechia

Related Links

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https://trialinfoemail.pfizer.com/pages/landing.aspx?StudyID=A5751032

To obtain contact information for a study center near you, click here.

Other Identifiers

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A5751032

Identifier Type: -

Identifier Source: org_study_id

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