Overview
A Study of Rheumatoid Arthritis Treatment With Enbrel in Adult Patient in Outpatient Department
Status:
Terminated
Terminated
Trial end date:
2013-01-01
2013-01-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This is an open-label, multicenter and observational study in China, which is designed to record the data of RA & AS patients within 52 weeks after rheumatologists decided to prescribe etanercept, and evaluate the safety and efficacy of the treatment. All eligible subjects agreed to be recruited in the study and can withdraw anytime if they choose so. Patients with RA or AS are typically managed by rheumatologists. As this study seeks to record the data of RA & AS patient in etanercept and evaluate the safety and efficacy of the treatment, patients will be recruited from Rheumatic department. Rheumatologist will be asked to build up the database for RA & AS patient surveillance prospectively in outpatient dept, which benefits for the patient treatment outcomes evaluation and clinical management.Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
PfizerTreatments:
Etanercept
Criteria
Inclusion Criteria:- Subject has a confirmed diagnosis of rheumatoid arthritis or ankylosing spondylitis.
- Subject has accepted physician's prescription of etanercept in rheumatology
department.
- Subject agreed to be enrolled in the observational study and sign the ICD.
- Subject is≥18 years of age at the time of consent.
- Subject is willing and able to understand and complete questionnaires
Exclusion Criteria:
- Presence of active or suspected latent infection including HIV, or any underlying
disease, including open cutaneous ulcers that could predispose the subject to
infections.
- Immunodeficiency syndromes including Felty syndrome or large granular lymphocyte
syndrome.
- Active tuberculosis (TB) or a history of TB, or findings consistent with previous
exposure to TB on a chest x-ray (CXR). Investigators must follow China's guidelines
for appropriate screening and treatment of TB.
- History of hypersensitivity to any of the ingredients in either preparation.