QuickVue Influenza A+B Clinical Field Trial

Quidel

Status: Completed

Conditions: Influenza

Treatments: Device: Swab Specimen Collection (QuickVue)

Study type: Interventional

Funder types: Industry

Identifiers

NCT00491283

CS-0119-08(B)

Details and patient eligibility

About

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

Sex: All

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: Single Blind