Last updated on December 2016

Registry for Analysis of Compliance in Colombian Participants With Rheumatoid Arthritis Exposed to Golimumab

Brief description of study

The purpose of this study is to describe adherence to golimumab in Colombian participants with rheumatoid arthritis (RA) experiencing adequate treatment response, in a real-world clinical settings.

Detailed Study Description

This is a multi-center (when more than one hospital or medical school team work on a medical research study), non-interventional, prospective cohort study that will enroll participants with RA in Colombia, for whom the treating physician has decided to treat with golimumab prior to enrolment. All participants will be observed for adherence to golimumab treatment for 24 months from study start (Week 0), and recommended follow up assessments will be every 3 months. Any changes including addition of new medications or dose modifications of existing medications will be entirely according to the treating physician's judgment. Participants' safety will be monitored throughout the study.

Clinical Study Identifier: NCT02414984

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Barranquilla, Colombia
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Bogota, Colombia
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Bogotá, Colombia
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Bucaramanga, Colombia
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Cali, Colombia
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Medellin, Colombia
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Medellín, Colombia
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Recruitment Status: Open

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