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Molecular biological and immunological determinants of severe RSV infections in children

Molecular biological and immunological determinants of severe RSV infections in children

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00036190
Enrollment
400
Registered
2025-03-18
Start date
2024-11-21
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

B97.4

Interventions

Group 1: Description of the local mucosal and the systemic immune response in the nose as the primary site of infection: a. Which cell populations dominate? Are there any differences to RSV-uninfected

Sponsors

Universitätsklinikum Düsseldorf
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: - Study participants are patients of the University Hospital Düsseldorf - Consent to participate in the study by the parents or legal guardians and consent to participation by the study participant (from pre-school age) - Symptoms indicative for a respiratory infection and/or PCR or POCT test positive for RSV (target group) or alternatively RSV PCR or POCT test negative for RSV (control group, preferably comparable in terms of age and previous illnesses)

Exclusion criteria

Exclusion criteria: - No consent to the study - Age =18 years - Study participation is not reasonable at this time for health reasons

Design outcomes

Primary

MeasureTime frame
Identification of immunological characteristics for severe RSV courses: - Differences in the immune cell population in the mucosa between RSV-infected and uninfected children - Changes in the early mucosal and the systemic immune response (e.g. altered gene expression of immune factors) Molecular biological characterization of RSV strains in severe vs. mild courses - Genotypic and phenotypic description of circulating virus strains - Possible identification of new virus clusters First indications of the occurrence of escape variants under the influence of nirsevimab

Secondary

MeasureTime frame
- Correlation between clinical parameters and immune/viral characteristics - Correlation between disease severity and individual parameters (e.g. age, previous illnesses, socio-economic aspects)

Countries

Germany

Contacts

Public ContactJörg Timm

Universitätsklinikum Düsseldorf

Joerg.Timm@med.uni-duesseldorf.de+49 211 81 12225

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026