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临床试验/NL-OMON51179
NL-OMON51179已完成4 期

Vaccine response against SARS-CoV-2 in patients with primary Sjögren*s syndrome - VaccineSS

niversitair Medisch Centrum Groningen0 个研究点目标入组 180 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
180

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 18-75 years
  • Written informed consent
  • Fulfilment of 2016 ACR-EULAR criteria (for pSS patients)
  • Female sex (for healthy volunteers)

排除标准

  • Confirmed SARS-CoV-2 infection (current or previous)
  • Women who are pregnant (self-reported, participants will be asked -when in
  • doubt- to perform a pregnancy test before study entry)
  • Current use of prednisone >10mg/day, conventional DMARDs (except
  • hydroxychloroquine) or biological DMARDS. Previous use of DMARDs >=6 months
  • before inclusion (>=12 months for rituximab) is allowed.

研究者

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