German Spondyloarthritis Inception Cohort

NCT01277419 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2021-10-12

No results posted yet for this study

Summary

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

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

Sponsors & Collaborators

  • German Federal Ministry of Education and Research

    collaborator OTHER_GOV
  • AbbVie

    collaborator INDUSTRY
  • Amgen

    collaborator INDUSTRY
  • Centocor, Inc.

    collaborator INDUSTRY
  • Schering-Plough

    collaborator INDUSTRY
  • Wyeth is now a wholly owned subsidiary of Pfizer

    collaborator INDUSTRY
  • Berlin Institute of Health

    collaborator OTHER
  • Novartis

    collaborator INDUSTRY
  • UCB Pharma

    collaborator INDUSTRY
  • Charite University, Berlin, Germany

    lead OTHER

Principal Investigators

  • Joachim Sieper, Prof. Dr. · Charite University, Berlin, Germany

  • Martin Rudwaleit, Prof. Dr. · Charite University, Berlin, Germany

  • Denis Poddubnyy, Prof. Dr. · Charite University, Berlin, Germany

  • Fabian Proft, MD · Charite University, Berlin, Germany

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-07-31
Primary Completion
2030-07-31
Completion
2030-07-31

Countries

  • Germany

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01277419 on ClinicalTrials.gov