Influenza Clinical Trial
Official title:
Clinical Performance of the Diassess Influenza A and B Test
Verified date | February 2018 |
Source | Diassess Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The primary objective of this study is device feasibility of the Diassess Influenza A and B Test
Status | Completed |
Enrollment | 567 |
Est. completion date | May 2017 |
Est. primary completion date | May 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Subject currently has a fever (=37.8°C/100°F), or self-reports having had or is currently treating a fever =37.8°C/100°F with onset within the previous 72 hrs - Subject has at least one additional flu-like symptom including fever or feeling feverish/chills, runny or stuffy nose, muscle or body aches, fatigue (very tired), sore throat, headaches, or cough Exclusion Criteria: - Subject received nasal vaccine (e.g. FluMist) within the past 10 days - Subject has been taking or took any antivirals for influenza in the past 30 days - Subject enrolled in any drug trials |
Country | Name | City | State |
---|---|---|---|
United States | University Health Care Center | Syracuse | New York |
Lead Sponsor | Collaborator |
---|---|
Diassess Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Diassess test measurement agreement with Polymerase Chain Reaction (PCR) | One (1) patient visit which is a time frame of one (1) hour |
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