An Observational Study of the Real Life Management of the Psoriasis Patients Treated With Enbrel According to the New Reimbursement Criteria
NCT ID: NCT01557283
Last Updated: 2014-06-30
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
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COMPLETED
140 participants
OBSERVATIONAL
2011-09-30
2013-06-30
Brief Summary
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To describe the average treatment duration of patients with Enbrel expressed as a number of weeks/year.
To describe the number of patients who receive continuous treatment To describe the number of patients who receive intermittent treatment To describe the number of weeks off treatment
Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Plaque psoriasis patients
Plaque psoriasis patients treated with Enbrel after the approval of the new belgian reimbursement criteria
Enbrel treatment
Enbrel SC 50mg once weekly or 25mg twice weekly
Interventions
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Enbrel treatment
Enbrel SC 50mg once weekly or 25mg twice weekly
Eligibility Criteria
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Inclusion Criteria
* Patients ≥18 year
* Evidence of a personally signed and dated informed consent document indicating that the subject (or a legally acceptable representative) has been informed of all pertinent aspects of the study.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Locations
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Herestraat 49
Leuven, , Belgium
Countries
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Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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BEFLEX
Identifier Type: -
Identifier Source: secondary_id
B1801314
Identifier Type: -
Identifier Source: org_study_id