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Chinese Spondyloarthritis Inception Cohort (CESPIC)

A

Army Medical University

Status

Not yet enrolling

Conditions

Reactive Arthritis (ReA)
Acute Anterior Uveitis (AAU)
Axial Psoriatic Arthritis (axPsA)
Non-radiographic Axial Spondyloarthritis (Nr-axSpA)
Ankylosing Spondylitis (AS) / Radiographic Axial SpA (r-axSpA)
Ulcerative Colitis (UC)
Crohn Disease (CD)

Treatments

Drug: Celecoxib

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The Chinese Spondyloarthritis Inception cohort (CESPIC) was started 2000 as a prospective, longitudinal, multicentre, nationwide study in China on patients with early SpA including ankylosing spondylitis (AS, also known as radiographic axial spondyloarthritis) and non-radiographic axial SpA. The objectives of CESPIC 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). CESPIC has been recently expanded to recruit patients with other forms of SpA / conditions associated with SpA: reactive arthritis, acute anterior uveitis, Crohn's disease as well as with psoriasis / axial psoriatic arthritis.

Enrollment

1,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

Crohn's disease. Acute anterior uveitis. Psoriatic arthritis with axial involvement. Reactive arthritis.

Exclusion criteria

Infections, Malignancies, Major cardiovascular events, Lower intestinal perforations Other adverse events

Trial design

1,000 participants in 7 patient groups

Ankylosing spondylitis
Description:
Ankylosing spondylitis according to the modified New York criteria or with the clinical diagnosis of AS/r-axSpA fulfilling the ASAS Classification Criteria AND the mNY criteria plus having the indiaction for starting a bDMARD therapy according to the treating rheumatologist
Treatment:
Drug: Celecoxib
Non-radiographic axial spondyloarthritis
Description:
Patients with clinical characteristics of axial SpA but not fulfilling the modified New York criteria for which radiographic sacroiliitis is essential or with the clinical diagnosis of nr-axSpA fulfilling the ASAS Classification Criteria not fulfilling the mNY criteria and the indiaction for starting a bDMARD therapy according to the treating rheumatologist
Treatment:
Drug: Celecoxib
Juvenile spondyloarthritis
Description:
Patients with juvenile spondyloarthritis (juvenile ankylosing spondylitis, juvenile non-AS-spondyloarthritis).
Treatment:
Drug: Celecoxib
Crohn's disease
Description:
Patients with Crohn's disease
Treatment:
Drug: Celecoxib
Acute anterior uveitis
Description:
Patients with acute anterior uveitis
Treatment:
Drug: Celecoxib
Axial psoriatic arthritis
Description:
Patients with the clinical diagnosis of psoriatic arthritis with axial involvement (sacroiliac joints and/or spine) (axPsA)
Treatment:
Drug: Celecoxib
Reactive arthritis
Description:
Patients with reactive arthritis
Treatment:
Drug: Celecoxib

Trial contacts and locations

0

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Central trial contact

Guangxing Chen, Ph.D.

Data sourced from clinicaltrials.gov

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