跳至主要内容
临床试验/NCT03444623
NCT03444623Unknown不适用

Survivin as Predictive Biomarker for Development of Rheumatoid Arthritis

Vastra Gotaland Region1 个研究点 分布在 1 个国家目标入组 6,000 人开始时间: 2013年6月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
6,000
试验地点
1
主要终点
Survivin positive

研究概览

简要总结

Purpose: to examine the possibility of using the onco-protein survivin as a predictive biomarker for identifying individuals at risk of developing rheumatoid arthritis within a cohort of patients seeking treatment for joint pain/stiffness. Secondly, to study survivin as a prognostic marker for joint destruction, refractory and highly active disease in patients with established RA.

详细描述

The study will analyse survivin levels in a non-selected material within a cohort of patients seeking help at their primary health care for joint pain, stiffness, swelling etc. Patients presenting with such symptoms (not explained by injury or other factors) are suspected to have an arthritic condition such as RA, and are routinely tested for presence of autoantibodies RF and ACPA. In this observational study we add measurement for survivin to the blood analyses of these patients. Information about patients expressing high levels of survivin will be reported to the referring doctor at the primary health care, and for patients not previously having been examined by a rheumatologist this will be offered.

The study will be performed at Sahlgrenska university hospital Gothenburg and Umeå university hospital.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients seeking treatment at the primary health care for problems with their joints (pain, stiffness).

排除标准

  • Patients diagnosed with RA

结局指标

主要结局

Survivin positive

时间窗: 1 year

Survivin positive: \> 0,45 ng/ml Survivin negative: \< 0,45 ng/ml

次要结局

未报告次要终点

研究者

发起方
Vastra Gotaland Region
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验