QuickVue Influenza A+B Clinical Field Trial

NCT ID: NCT00491283

Last Updated: 2008-01-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2006-07-31

Study Completion Date

2006-08-31

Brief Summary

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A comparative study of different swab types used for collection of specimens for rapid inluenza testing

Detailed Description

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Conditions

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Influenza

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

SINGLE

Interventions

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Swab Specimen Collection (QuickVue)

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

Subjects must have:

* Fever (\>38°C) (at time of visit or within the previous 48 hrs by history) and at least two of the following symptoms:

* Chills/sweats
* Cough
* Dyspnea (labored, difficult breathing)
* Fatigue
* Headache
* Myalgia (deep muscle aches)
* Nasal congestion
* Runny nose
* Sore throat

Exclusion Criteria

* Patients who are undergoing treatment with antivirals, now or within the last 7 days cannot be included in this study.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Quidel Corporation

INDUSTRY

Sponsor Role lead

Principal Investigators

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Andrew Keller, MD

Role: PRINCIPAL_INVESTIGATOR

Sydney Airport medical Centre

Locations

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Sydney Airport Medical Centre

Mascot, New South Wales, Australia

Site Status

Countries

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Australia

Other Identifiers

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CS-0119-08(B)

Identifier Type: -

Identifier Source: org_study_id

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