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Comparison of Nylon Flocked Swabs and Saline Aspirates for Detection Respiratory Viruses

Comparison of Nylon Flocked Swabs and Saline Aspirates for Detection Respiratory Viruses

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00613184
Enrollment
150
Registered
2008-02-12
Start date
2006-11-30
Completion date
2008-01-31
Last updated
2008-02-12

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

Conditions

Bronchiolitis, Human Metapneumovirus, Influenza, Pediatric, Respiratory Syncytial Virus

Keywords

Respiratory Syncytial virus, Bronchiolitis, Pediatric

Brief summary

Collection of nasal secretions from infants and toddlers for viral testing is usually done using the nasal washing technique described by Hall in 1975. This is cumbersome. Previous attempts to use swabs have been unsuccessful because the swabs didn't work well. A newly designed swab may work better and in this study we compare the new swab with the old style nasal washing. .

Detailed description

Collection of nasal secretions from infants and toddlers for viral testing is typically performed using the nasal saline aspirate technique described by Hall in 1975. Nylon flocked swabs (NFS) and universal transport medium for room temperature (UTM-RT) (Copan Medical, Murrieta, CA) storage media have been found to be an effective collection and transport method for bacteria causing sexually transmitted infections. We adapted these swabs and storage medium to collect respiratory viruses from children less than18 months old and compared detection rates using NFS and traditional nasal aspirates. We will determine the relative roles of the UTM-RT and NFS release and therefore measured viral detection rates of common respiratory pathogens in traditional saline aspirates stored in UTM-RT. Our primary hypothesis is that nasal secretions collection using NFS stored in UTM-RT will lead to a higher detection rate of the respiratory viruses we arestudying; namely RSV, Influenza and human metapneumovirus from than collection of unpreserved saline nasal aspirates in children less than 18 months of age.

Interventions

DEVICENylon Flocked swab (Nasal secretion sampling)

Nasal Aspirate Nylon Flocked swab

Sponsors

Medical Diagnostic Laboratories, LLC
CollaboratorINDUSTRY
Copan Innovation Murrietta, CA
CollaboratorUNKNOWN
Kern Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Months
Healthy volunteers
No

Inclusion criteria

* Treating clinican ordered RSV antigen testing

Exclusion criteria

* Refusal of consent * Age \> 18 months

Design outcomes

Primary

MeasureTime frame
Viral detection rate by PCR0 not applicable

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026