Influenza, Human, Respiratory Syncytial Virus Infections
Conditions
Brief summary
A Multicenter Study Conducted to Evaluate the Performance of the LumiraDx Influenza A/B + RSV Test at Point of Care Testing Sites
Detailed description
The LumiraDx Influenza A/B + RSV Test is a rapid microfluidic immunofluorescence assay for use with the LumiraDx instrument for the qualitative detection and differentiation of Influenza type A, Influenza type B and respiratory syncytial virus (RSV) viral antigens. The test is not intended to detect influenza C antigens. The LumiraDx Influenza A/B + RSV assay uses nasal swabs or nasopharyngeal swab specimens, collected from symptomatic patients. Approximately 2000 subjects will be enrolled in this study. 120 influenza A positive, 120 influenza B positive and 120 RSV positive samples are required, in addition to at least 120 samples negative for influenza and 120 negative RSV samples, representing four (4) age groups: ≤ 5 years, 6 to 21 years, 22 to 59 years, and ≥ 60 years. Depending on the prevalence of influenza A, influenza B or RSV, it will be necessary to collect a significantly higher number of total samples to obtain the required number of positives. Banked specimens may be used to supplement the data set. The objectives of this clinical study are twofold: * Evaluate the performance of the LumiraDx Influenza A/B + RSV Test in detecting and differentiating influenza A, influenza B and RSV in fresh nasal or nasopharyngeal swab specimens from patients with signs and symptoms of influenza and or RSV-like illness, as compared with an FDA-cleared comparative method. * Evaluate LumiraDx Influenza A/B + RSV Test performance when the test is run by non-laboratory users in point-of-care (POC) locations representative of sites who perform testing under a CLIA certificate of waiver.
Interventions
DIAGNOSTIC_TESTSwab
Swab samples for diagnostic test
Sponsors
LumiraDx UK Limited
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* The subject may be of any age and either sex. * Preliminary assessment of the subject by the Investigator/designee should be suggestive of influenza and/or RSV at the time of the study visit. The subject must exhibit two (2) or more of the following signs and symptoms for eligibility: stuffy or runny nose, sneezing, cough, sore throat, dyspnea (labored, difficult breathing), wheezing, fatigue, weakness and/or malaise, arthralgia (joint pain), myalgia (deep muscle aches), anorexia, vomiting, diarrhea, or headache. The onset of these symptoms must not have begun more than four (4) days prior to study enrollment. * The subject must have a fever of 100.0 °F or greater with the onset of the fever being within the past three (3) days and/or present at the time of the visit. Fever can be reported or taken at time of visit. Subjects 18 years and older must report having a fever, but a quantitative reported measurement is not necessary for inclusion.
Exclusion criteria
* The subject underwent a nasal wash/aspirate as part of standard of care testing during this study visit. * The subject is undergoing treatment currently and/or within the past 14 days of the study visit with an inhaled influenza vaccine (FluMist®) or anti-viral medication, which may include but is not limited to Amantadine (Symmetrel®), Rimantadine (Flumadine®), Zanamivir (Relenza®), Oseltamivir (Tamiflu®), or Baloxavir Marboxil (Xofluza™). * The subject is undergoing treatment currently or had undergone within the past 14 days of the study visit with RSV-related medication which may include but is not limited to Ribavirin (Virazole), RSV-IGIV (RespiGam) or palivizumab (Synagis). * The subject is currently receiving or has received within the past thirty (30) days of the study visit an experimental biologic, drug, or device including either treatment or therapy. * The subject has previously participated in this research study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Performance evaluation by health care professionals | 4 months | Evaluate the performance of the LumiraDx Influenza A/B + RSV Test in detecting and differentiating influenza A, influenza B and RSV in fresh nasal or nasopharyngeal swab specimens from patients with signs and symptoms of influenza and or RSV-like illness, as compared with an FDA-cleared comparative method. |
| Performance evaluation by non-laboratory users | 4 months | Evaluate LumiraDx Influenza A/B + RSV Test performance when the test is run by non-laboratory users in point-of-care (POC) locations representative of sites who perform testing under a CLIA certificate of waiver. |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORChristina Ulen
Advanced Pediatrics
PRINCIPAL_INVESTIGATORRobert Rosen
Ardmore Family Practice
PRINCIPAL_INVESTIGATORRamin Farsad
Access Medical Center
PRINCIPAL_INVESTIGATORMatthew Morgan
Centura Health Physician Group
PRINCIPAL_INVESTIGATORJeffrey Stewart
Family Medical Associates
PRINCIPAL_INVESTIGATORAndre Gvozden
Gvozden Pediatrics
PRINCIPAL_INVESTIGATORIsaac Melamed
ImmunoE Health Center
PRINCIPAL_INVESTIGATORNader Nakhleh
Jersey Shore UMC
PRINCIPAL_INVESTIGATORLisa Connery
Lisa Connery MD
PRINCIPAL_INVESTIGATORAftab Naz
Madera Family Medical Group
PRINCIPAL_INVESTIGATORSalma Elfaki
Nona Pediatric Center
PRINCIPAL_INVESTIGATORAdam Kaplan
North Texas Family Practice
PRINCIPAL_INVESTIGATORPaul Wisman
Pediatric Research of Charlottesville
PRINCIPAL_INVESTIGATORWilliam Simon
New Medical Healthcare
PRINCIPAL_INVESTIGATORJoshua Fuller
Pediatric Care
PRINCIPAL_INVESTIGATORDavid King
Southwest Care
PRINCIPAL_INVESTIGATORSong Yu
MedHelp Urgent Care
PRINCIPAL_INVESTIGATORMichael Bell
Accel-West Volusia Pediatrics
Outcome results
None listed