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SARS-CoV-2 detection in saliva samples (SDS)

Not Applicable
Conditions
Sensitivity/specificity of the Lolli method for the detection of respiratory viruses
Registration Number
DRKS00032803
Lead Sponsor
Institut für Virologie, Uniklinik Köln
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
490
Inclusion Criteria

Consent from the subject or both legal guardians
- Consent from the children, provided they are capable of giving consent themselves (from around 14 years of age)
- Declaration of intent for children under 14 years of age
- Good physical condition (Karnofsky index =80%)
- PCR confirmed infection with one of the mentioned respiratory viruses in the last 21 days and/or clinical or epidemiological suspicion of infection (symptoms of infection with a respiratory virus: cough, runny nose, fever, chills and/or association with a known wave of infections with a respiratory virus)
- PCR confirmed negative subjects

Exclusion Criteria

- No ability to consent
- Refusal to participate
- Employment at the Institute of Virology, University Hospital Cologne

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Virus detection in saliva samples
Secondary Outcome Measures
NameTimeMethod
Differences in virus concentration in nasal/throat swabs compared to saliva samples, assessment of the different saliva collection methods
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