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临床试验/NCT04364828
NCT04364828已完成不适用

NGS Diagnostic in COVID-19 Hosts - Genetic Cause Relating to the Course of Disease Progression

University Hospital Tuebingen1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2020年10月21日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
1,000
试验地点
1
主要终点
Viral evolution

研究概览

简要总结

In this study (i) the host genome to identify susceptibility regions of infection, inflammation, and host defense, (ii) host response to Severe Acute Respiratory Syndrome-Corona-Virus-2 (SARS-CoV-2) infection, and (iii) viral sequence composition to define viral sequences which may be correlated with disease severity in addition to the metagenome of the throat swab will be analysed .

详细描述

This study aims to recruit adult persons with diagnostically confirmed Corona-Virus- Disease-19 (COVID-19) infection and with different disease manifestation who are included into diagnostic or therapeutic care at the University Hospital Tübingen (UKT).

The COVID-19 Next-Generation-Sequencing (NGS) study aims to cover as many patients in Germany as possible. It is expected to include in Phase 1 (pilot study): 250 patients with different disease manifestation (extreme phenotypes) and individual risk factors by whole genome analysis Phase 2 (verification study): 1.000 clinically well-defined patients to ensure a broader range of overlapping phenotypes, to verify data from the pilot study.

Phase 3 (confirmation study): > 10.000 patients to increase the power (anticipated).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •COVID-19 infection confirmed
  • •COVID-19 disease manifestation
  • •Age > 18 years

排除标准

  • •Missing informed consent of the patient/ legal guardian/ relatives

研究组 & 干预措施

Host Genome Analysis

Other

For 150 patients from the extreme phenotypes - complementary to Whole Genome Analysis of each patient also Whole Transcriptome will performed Analysis; DNA methylation analysis using EPIC arrays will be performed in the pilot study (phase 1). Identically, in phase 2 starting from month 4, will be generated WGS, Whole transcriptome sequencing (WTS), and methylation data of the 500 patients. Epigenetic changes are likely to occur upon Corona infection. Subsequently, genome and epigenome data with RNA expression pattern will be correlated.

干预措施: Whole Genome Analysis (Genetic)

Host Response to SARS-CoV-2 Infection

Other

Focus on longitudinal analysis of TCR repertoire of CD4+ and CD8+ T cells from blood samples (PBMCs) from clinically characterized patients (n = 24). The bulk- T-cell receptor (TCR) sequencing will be performed at different time points during the course of disease progression and recovery.

干预措施: T-cell receptor (TCR) repertoire (Genetic)

Viral Sequence Composition

Other

The Severe Acute Respiratory Syndrome-Corona Virus-2 (SARS-CoV-2) viral composition is determined by Next Generation sequencing (different protocols for enrichment are available, and are currently being tested to successfully analyse the virus from different isolates). It is known that SARS-CoV-2 sequence is changing at least one position every second passing from person to person. Numerous variants have been described deriving from 3 different ancestral viruses (named A, B, and C) reflecting different distributions in East Asia, Europeans and Americans. At it is anticipated that other (super)infections may add to the severity of the infection and disease course, the entire metagenome of the throat is being sequenced and analyzed as well.

干预措施: SARS-CoV-2 viral composition (Genetic)

结局指标

主要结局

Viral evolution

时间窗: Day 1, Day 3-5, Day 7-9, 48 hours after recovery

The change in the genetic makeup of a virus population (measured in numbers) as the viruses mutate and multiply over time at different time points

次要结局

  • Immune response(Day 1, Day 3-5, Day 7-9, 48 hours after recovery)
  • Disease severity(Day 1, Day 3-5, Day 7-9, 48 hours after recovery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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