The Rhinovirus Hospitalization and Investigation of Nasal-airway Omics (RHINO) Study

ConditionRhinovirus
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 17
SponsorUniversity of Wisconsin, Madison

About this trial

The goal of this study is to determine the burden of Rhinoviruses (RVs) as a cause of acute, severe, respiratory illnesses leading to hospitalization. A community cohort of 120 children between 12 and 36 months of age will be enrolled in the first year of the study and followed (when well and sick) for 36 months to identify the circulating RVs and provide samples to establish a host nasal transcriptome differentiating clinical from subclinical RV infections. A hospitalized cohort of 450 infants and children will be enrolled during years 1 through 3 of the study and followed for the duration of their hospitalization to investigate the findings of the community cohort. An additional 100 healthy children aged 5-17 years will be enrolled for age-match comparison with the older hospitalized cohort.

Eligibility criteria

Qualifiers

Parent/legal guardian is willing and able to provide informed consent in English.

Willing to comply with all study procedures and be available for the duration of the study.

Younger Community Group: Generally healthy children 12 to 36 months of age at the time of enrollment

Older Community Group: Generally healthy children 5 to 17 years of age at the time of enrollment.

Disqualifiers

Congenital or currently acquired immunosuppressive condition or medications (e.g., congenital immunodeficiency, Leukemia, Lupus)

Congenital anomalies that might alter frequency of infection (e.g., unrepaired cleft palate, bronchial cyst, pulmonary sequestration)

Presence of tracheostomy or gastrostomy tube

Previously enrolled a different group in the study

Trial design

Treatments tested in this trial

  • Nasal Swab Healthy Surveillance
  • Nasal Swab Sick Samples
  • Nasal Swab Hospitalized Cohort
  • Sick Follow-up Survey
  • Older Cohort Control Group

Treatment groups

670 Participants
are divided into 3 treatment groups

Sponsors and collaborators

University of Wisconsin, Madison

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Collaborator