NL-OMON50071已完成不适用
Cellular & Serological Immune Response Monitoring in SARS-CoV2-infected individuals, without need of hospitalization - SARS-RESPONSE
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational invasive
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Subject (male or female) tested positive for SARS-CoV2 by PCR (nasal swab,
- •throat swab and/or sputum);
- •Subject is an adult of 18-65 years old;
- •Subject is able to understand the PIF document, written in Dutch;
- •Subject is able to communicate well with the investigator in the Dutch
- •Subject signed informed consent prior to any study-mandated procedure;
- •Subject is living in Leiden or direct environment (e.g. within 10 km from
- •LUMC), allowing for traveling by car, bike or by walking to LUMC (no public
- •transportation).
排除标准
- •Subject tested negative upon SARS-CoV2 PCR re-analysis of nasal swab at
- •Subject previously fainted before, during or after a medical procedure with
- •Subject received plasma or other blood products during the previous 3 months;
- •Subject received a vaccination during the previous 3 months;
- •Subject is obese with BMI >=30, based on provide weight and length information;
- •Subject has a pre-existing coagulopathy;
- •Subject uses medication for a coagulopathy;
- •Subject uses medication that suppresses the immune system;
- •Subject has an auto-immune disease or another immune disease;
- •Subject has another infection in addition to the SARS-CoV2 infection;
- •Subject participated in a clinical trial within 6 months prior to this study;
- •For women: subject is pregnant or is providing breast-feeding.
研究者
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