QuickVue Influenza A+B Clinical Field Trial

Not Applicable

Completed

• Conditions: Influenza

• Registration Number: NCT00491283
• Lead Sponsor: Quidel Corporation

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2006-07
• Primary Completion: 2006-08
• Study Completion: 2006-08
• Study First Submitted: 2007-06-22
• Study First Submitted QC: 2007-06-25
• Study First Posted: 2007-06-26
• Status Verified: 2008-01
• Last Update Submitted: 2008-01-23
• Last Update Posted: 2008-01-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: Not specified

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Sensitivity and Specificity	five months

Secondary Outcome Measures

Name	Time	Method
Sensitivity and Specificity	Positive and Negative Predictive Values

Trial Locations

Locations (1)

Sydney Airport Medical Centre; 🇦🇺 Mascot, New South Wales, Australia