A Study to Validate a New Oral Fluid/Saliva Antibody Test for Novel H1N1v Influenza

At present influenza immunity can only be reliably confirmed by a blood test. This test is invasive for the patient. This study is intended to validate an oral fluid/saliva antibody test for the variant Swine Influenza H1N1. If such a test were available, this painless and non invasive test will improve direct clinical care to an individual as well as significantly help guide future public health management of the pandemic.

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Key information

Conditions

H1N1 Virus Infections Orthomyxoviridae Infections RNA Virus Infections Virus Diseases

Age range

6 month and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Participants of the clinical service evaluation of novel H1N1v vaccine
First or second blood sample for the clinical service evaluation successfully collected

Exclusion criteria

Withdrawn from clinical service evaluation of novel H1N1v vaccine
Second blood sample for the clinical service evaluation not collected.

Sponsors and collaborators

Lead sponsor

Public Health England

Other Gov

Registry information

Acronym: Snuffles

Important dates

Study start: 2010
Primary completion: 2010
Study completion: 2010
First posted: Sep 1, 2010
Registry last updated: Sep 1, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed