Ignite Creation Date:
2024-05-06 @ 7:25 PM
Last Modification Date:
2024-10-26 @ 3:06 PM
Study NCT ID:
NCT06008457
Status:
COMPLETED
Last Update Posted:
2024-05-09
First Post:
2023-08-21
Brief Title:
Evaluation of the Labcorp COVID-19FluRSV Test Home Collection Kit
Sponsor:
Sequenom Inc
Organization:
Sequenom Inc
Study Overview
Official Title:
Prospective Clinical Evaluation of the Labcorp COVID-19FluRSV Test Home Collection Kit as Offered Commercially by Labcorp - A Registry Study
Status:
COMPLETED
Status Verified Date:
2023-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
To compare the results obtained by analysis of a self-collected anterior nasal AN swab as part of the Labcorp COVID-19FluRSV Test Home Collection Kit to a healthcare provider HCP-collected AN swab in patients with symptoms of viral respiratory infection consistent with influenza A Flu A influenza B Flu B respiratory syncytial virus RSV andor SARS-CoV-2 C-19
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None