跳至主要内容
临床试验/NCT03214263
NCT03214263招募中不适用

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

Rigshospitalet, Denmark11 个研究点 分布在 1 个国家目标入组 20,000 人开始时间: 2015年5月最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
20,000
试验地点
11
主要终点
To predict treatment effectiveness and tolerability for the individual patient

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with or suspected for the following diseases: rheumatoid arthritis (RA), psoriatic arthritis (PsA), axial spondyloarthritis (axSpA) or other inflammatory rheumatic diseases, connective tissue disorders or gout
  • Aged 18 year or older
  • Able to give informed consent

排除标准

  • 未提供

结局指标

主要结局

To predict treatment effectiveness and tolerability for the individual patient

时间窗: At treatment onset and at 3, 6, 12, 24, 36, 48 and 60 months

Number of patients that achieve a standardized treatment response and do not experience serious adverse events

To diagnose inflammatory rheumatic diseases early in the disease course with high specificity and sensitivity

时间窗: Changes from baseline to 3, 6, 12, 24, 36, 48, and 60 months

Number of patients suspected of rheumatoid arthritis, axial spondyloarthritis, psoriatic arthritis, gout or connective tissue diseases that can be correctly diagnosed

To improve prognostication

时间窗: At diagnosis and after 3, 6, 12, 24, 36, 48 and 60 months

Number of patients that can be correctly prognosticated by progression in physical function (by HAQ) and in bone damage (by imaging)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Merete L Hetland

Professor

Rigshospitalet, Denmark

研究点 (11)

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