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临床试验/NCT05212766
NCT05212766招募中不适用

Role of the Oral Microbiome & Mucosal Immunity in COVID-19 Disease: Diagnostic/Prognostic Utility in South Asian Populations

King's College London1 个研究点 分布在 1 个国家目标入组 750 人开始时间: 2022年4月7日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
750
试验地点
1
主要终点
Relationship between oral mucosal immunity and microbiome on COVID outcomes in different ethnic groups

研究概览

简要总结

Determining whether in the mouth there are differences between the participant groups in the nature and activity of mucosal innate immunity, in immune responses to SARS-COV2 antigens, or in the oral microbiome

详细描述

Cross sectional with longitudinal component

  • Stimulated whole mouth fluid (SWMF) and blood samples from South Asian and non-Asian populations
  • Controls, and COVID-19 patients in both populations.
  • Oral disease questionnaire and clinical examination
  • Separation of SWMF into pellet for DNA extraction for microbiomics and supernatant for cell phenotype analysis, cytokines and antibodies to SARS-CoV2 antigens

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • • South Asian and White British persons and those diagnosed with symptomatic or asymptomatic COVID-19 infection.
  • Aged 18 or over. Able to understand and consent.
  • Uninfected subjects: no history of COVID-19; not vaccinated; (negative for anti-SARS-CoV2 nucleoprotein antibodies at lab)
  • For patient groups: Confirmed COVID-19 positivity, symptoms and symptom onset within the past 21 days; Be recently hospitalised with COVID-19 disease; Have COVID-19 disease proven by PCR testing for SARS-CoV-2 within the last 21 days; COVID disease severity graded as per NIH/WHO.
  • Recovered groups: Have had COVID-19 disease proven by PCR testing for SARS-CoV-
  • COVID disease severity graded as per WHO or NIH equivalent criteria
  • Those willing to participate on a single occasion but unwilling to participate with longitudinal samples will not be excluded.
  • Smoking, obesity, diabetes, heart disease, antibiotics or treatment related to COVID is not excluded.

排除标准

  • • Those patients unwilling to participate, those unable to understand sufficiently to give informed consent and those unable to participate due to the severity of COVID-19 disease. Those patients classified as not either South Asian or White British heritage.
  • Patients with malignancy, pregnancy, long term immune suppression, inability to give informed consent, not willing or able to have oral examination.
  • Diabetes not excluded but screening for diabetes will be performed: glucose will be assessed in blood/serum sample (150ul).
  • Exclusion criteria summary:
  • Critically ill participants who cannot give informed consent
  • Those who are not willing to have an oral examination, or donate blood or saliva samples.
  • Those who cannot chew / drool to provide a SWMF sample due to severe/critical medical conditions
  • Participants with known malignancies or who are pregnant
  • Participants who are on long-term immunosuppressants (e.g. for autoimmune diseases)
  • Participation in other current research that is designed to, or is expected to alter the immune response.
  • Inability to communicate, understand or read English.

结局指标

主要结局

Relationship between oral mucosal immunity and microbiome on COVID outcomes in different ethnic groups

时间窗: 16 weeks

Multiple assessments

次要结局

  • Impact of pre-existing oral disease(16 weeks)
  • Impact of immunity and oral microbiome(16 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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