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Identification of New Biomarkers to Improve Diagnostics or Predict Treatment Responses, Adverse Events or Prognosis in Patients With Inflammatory Rheumatic Disease Followed in the Danish Nationwide Quality Registry, DANBIO
Introduction: The medical treatment of inflammatory rheumatic diseases has improved dramatically during the last decades primarily due to the introduction of biological disease modifying anti-rheumatic drugs (bDMARDs). However, bDMARD treatment failure occurs in 30-40% of patients due to lack of effectiveness or side effects. The tools to predict treatment outcomes in the individual patient are currently limited. The objective of the present study is to identify diagnostic, prognostic and predictive biomarkers, which can be used to 1) diagnose inflammatory rheumatic diseases early in the disease course with high specificity and sensitivity, 2) improve prognostication or 3) predict treatment effectiveness and tolerability for the individual patient. Methods and analysis: Observational and translational open cohort study with prospective collection of clinical data and biological materials in patients with inflammatory rheumatic diseases treated in routine care. Patients contribute one cross-sectional blood sample (i.e. whole blood, serum, EDTA-plasma and -buffy coat, and blood in PAXgene RNA tubes) and/or are enrolled for longitudinal follow-up upon start of new DMARD (blood sampling after 0/3/6/12/24/36/48/60 months' treatment). Demographics, disease characteristics, comorbidities and lifestyle factors are registered at inclusion; DMARD treatment and outcomes are collected repeatedly during follow-up. Currently (June 2017) \>5,000 samples from ≈3,000 patients have been collected. Data will be analysed using appropriate statistical analyses. Ethics and dissemination: The protocol is approved by the Danish Ethics Committee and The Danish Data Protection Agency. All participants give written informed consent. Biomarkers will be evaluated and published according to REMARK, STROBE and STARD guidelines. Results will be published in peer-reviewed medical journals and presented at international conferences.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Department of Rheumatology, Aalborg University Hospital
Aalborg, Denmark
Department of Rheumatology, Aarhus University Hospital
Aarhus, Denmark
Department of Rheumatology, Rigshospitalet
Copenhagen, Denmark
Dept. of Rheumaology, University Hospital Bispebjerg and Frederiksberg
Copenhagen, Denmark
Dept. of Rheumaology, North Denmark Regional Hospital
Hjørring, Denmark
Department of Rheumatology, Zealand University Hospital Køge
Køge, Denmark
Department of Rheumatology, Odense University Hospital
Odense, Denmark
Dept. of Rheumaology, Randers Regional Hospital
Randers, Denmark
Department of Rheumatology, Svendborg Hospital
Svendborg, Denmark
Danish Arthritis Hospital
Sønderborg, Denmark
Start Date
May 1, 2015
Primary Completion Date
December 1, 2024
Completion Date
December 1, 2024
Last Updated
January 9, 2024
20,000
ESTIMATED participants
Lead Sponsor
Rigshospitalet, Denmark
Collaborators
NCT07295509
NCT06100744
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04402086