Influenza Clinical Trial
Official title:
Comparison of Swab Types for Specimen Collection
Verified date | January 2008 |
Source | Quidel Corporation |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
A comparative study of different swab types used for collection of specimens for rapid inluenza testing
Status | Completed |
Enrollment | 0 |
Est. completion date | August 2006 |
Est. primary completion date | August 2006 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
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. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Diagnostic
Country | Name | City | State |
---|---|---|---|
Australia | Sydney Airport Medical Centre | Mascot | New South Wales |
Lead Sponsor | Collaborator |
---|---|
Quidel Corporation |
Australia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Sensitivity and Specificity | five months | ||
Secondary | Sensitivity and Specificity | Positive and Negative Predictive Values |
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