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临床试验/ISRCTN52952998
ISRCTN52952998已完成未知

ong-term follow up of patients who participated in previous Vasculitis trials

Skane University Hospital Malmö-Lund, Sweden0 个研究点目标入组 875 人开始时间: 2010年5月7日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
875

研究概览

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • Current participant inclusion criteria as of 11/07/2019:
  • 1. Patients with newly diagnosed Anti-Neutrophil Cytoplasm Antibody Vasculitis recruited into one of EUVAS’ randomized controlled trials, NORAM, CYCAZAREM, MEPEX, CYCLOPS, RITUXVAS, IMPROVE, MYCYC performed by European Vasculitis Society (EUVAS)
  • Previous participant inclusion criteria:
  • 1. Patients with newly diagnosed Anti-Neutrophil Cytoplasm Antibody Vasculitis recruited into one of four randomised controlled trials, NORAM, CYCAZAREM, MEPEX, CYCLOPS performed by European Vasculitis Study Group
  • 2. The patients were recruited during the period of 1995 to 2002

排除标准

  • 1. Patients withdrawn from original study due to incorrect diagnosis
  • 2. Consent withheld by patient

研究者

发起方
Skane University Hospital Malmö-Lund, Sweden

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