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临床试验/NCT04005625
NCT04005625已完成不适用

Features of Microcrystalline Polyarthritis Treated by Biologics and Evolution - FUMBLE Study

University Hospital, Brest1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2019年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
46
试验地点
1
主要终点
Treatment duration

研究概览

简要总结

The study will involve adult patient who had received any biologic agent for microcrystalline disease in western France (Tours, Le Mans, Orléans, Angers, Rennes, Poitiers et Brest) between 01/01/2010 and 31/12/2018.

Investigators will answer retrospectively a questionnaire that covers patient and disease data, biologic agent use, efficacy and adverse events.

详细描述

This is a retrospective multicentric study of all patients treated by biologic for microcrystalline disease in France in western France (Tours, Le Mans, Nantes, La Roche sur Yon, Orléans, Angers, Rennes, Poitiers et Brest) between 01/01/2010 and 31/12/2018.

The investigators will collect all clinical (diagnosis of gout CCPD or hydroxyapatitis, tender and swollen joint count), biological (blood results: ESR, CRP, uric acid, synovial analysis), radiological data (X-rays performed and their description) .

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Crystal- induced arthritis
  • Treatment by biologic
  • In western France

排除标准

  • 未提供

结局指标

主要结局

Treatment duration

时间窗: one year

Duration of treatment by biologic in days

次要结局

  • number of synovitis(inclusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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