Actively Recruiting
German Spondyloarthritis Inception Cohort
Led by Charite University, Berlin, Germany · Updated on 2021-10-12
1000
Participants Needed
1
Research Sites
1565 weeks
Total Duration
On this page
Sponsors
C
Charite University, Berlin, Germany
Lead Sponsor
G
German Federal Ministry of Education and Research
Collaborating Sponsor
AI-Summary
What this Trial Is About
The German Spondyloarthritis Inception cohort (GESPIC) was started 2000 as a prospective, longitudinal, multicentre, nationwide study in Germany on patients with early SpA including ankylosing spondylitis (AS, also known as radiographic axial spondyloarthritis) and non-radiographic axial SpA. The objectives of GESPIC are to learn about the course of SpA during the very early stage of the disease, to appropriately assess the outcome including radiographic progression of patients after several years of follow-up, to identify outcome predictors, to assess quality of life, function, and costs (direct and indirect costs). GESPIC has been recently expanded to recruit patients with other forms of SpA / conditions associated with SpA: acute anterior uveitis, Crohn's disease as well as with psoriasis / axial psoriatic arthritis.
CONDITIONS
Official Title
German Spondyloarthritis Inception Cohort
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with definite diagnosis of axial spondyloarthritis or juvenile spondyloarthritis
- Patients with definite diagnosis of Crohn's disease
- Patients with definite diagnosis of acute anterior uveitis
- Patients with definite diagnosis of psoriatic arthritis with axial involvement
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
Charité - Universitätsmedizin Berlin
Berlin, Germany
Actively Recruiting
Research Team
D
Denis Poddubnyy, Prof. Dr.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
6
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