Study To Evaluate The Efficacy And Long-Term Adherence Of Spondyloarthropathies(SpA) Patients On Enbrel
- Registration Number
- NCT04507776
- Lead Sponsor
- Pfizer
- Brief Summary
This study is to evaluate local data in Iraqi patients with Spondyloarthropathies on Enbrel treatment with regards to efficacy and adherence using data from the Baghdad Teaching Hospital (Rheumatology Center)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 763
Inclusion Criteria
- Diagnosed SpA patients
- 18 years of age and older.
- Did not receive previous other biological treatments.
- Patients have at least 1 year on Enbrel.
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Exclusion Criteria
- Had previously used another biological treatments.
- Use of etanercept for less than 1 year duration.
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Patients with spondyloarthropathies Etanercept Patients with spondyloarthrosis that received Etanercept as treatment for disease
- Primary Outcome Measures
Name Time Method Percentage of Participants With 7 Years Adherence to Etanercept 7 years [from the data retrieved and observed in 1 month of this study] In this outcome measure, percentage of participants who continued etanercept treatment and adhered to the treatment for 7 years were reported.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Pfizer
🇮🇶Baghdad, Iraq