跳至主要内容
临床试验/NL-OMON56632
NL-OMON56632招募中不适用

AntiPhosphoLipid antibodies and point-of-care INR measurement with CoaguChek - VervOlg Studie - APLIVOS

niversitair Medisch Centrum Utrecht0 个研究点目标入组 44 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
44

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Age 18 years and older
  • - Previously confirmed APS, diagnosed in accordance with the Sydney criteria
  • - High titers of anti-B2-glycoprotein-I IgG at screening (titer > 99th
  • percentile)
  • - Lupus anticoagulant positive at screening
  • - Receiving VKA during at least 3 months
  • - At least one thromboembolic event in the past
  • - Willing and be able to understand the study information and sign the informed
  • consent form

排除标准

  • Patients with only obstetric complications of antiphospholipid syndrome without
  • thrombotic events

研究者

发起方
niversitair Medisch Centrum Utrecht

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