跳至主要内容
临床试验/EUCTR2021-000868-30-NL
EUCTR2021-000868-30-NL进行中(未招募)1 期

The immune-response and safety of COVID-19 vaccination in patients with chronic kidney disease, on dialysis, or living with a kidney transplant - The RECOVAC IR study

RECOVAC consortium0 个研究点目标入组 850 人开始时间: 2021年2月17日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
850

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. All patients should be eligible for COVID-19 vaccination as described by the instructions of the manufacturer.
  • 2. Age of 18 years or older
  • 3. Capable of understanding the purpose and risks of the study, fully informed and given written informed consent (signed informed consent form has been obtained)
  • - CKD4/5, with an eGFR <30 ml/min*1.73m2 by CKD-EPI
  • - Hemodialysis, or peritoneal dialysis
  • - Kidney transplant recipient at least 6 weeks after transplantation
  • - Partner, sibling, or other family member of participating patient with eGFR > 45 ml/min * 1,73 m2
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 570
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 280

排除标准

  • -History of severe adverse reaction associated with a vaccine and/or severe allergic reaction (eg, anaphylaxis) toany component of the study intervention(s).
  • -Multi-organ recipients
  • -Previous or active COVID-19 disease
  • -Active (haematological) malignancy
  • -Inherited immune deficiency
  • -Infection with Human Immunodeficency Virus (HIV)
  • -Bleeding diathesis or condition associated with prolonged bleeding that would, in the opinion of the investigator, contraindicate intramuscular injection.

研究者

发起方
RECOVAC consortium

相似试验