Impact of Swab Site and Sample Collector on Testing Sensitivity for COVID-19 Virus in Symptomatic Individuals
Completed
Conditions studied: Infections, Respiratory, Fever, Cough
In brief
Operational project to compare clinician collected nasopharyngeal (NP) samples to patient-obtained tongue, nasal and mid-turbinate (MT) samples in the detection of SARS-CoV-2 in an outpatient clinic setting
Key facts
- Study ID
- NCT04321369
- Run by
- UnitedHealth Group
- People needed
- 530
- Starts
- 2020-03-09
- Expected to finish
- 2020-03-23
- Last updated by the study team
- 2022-05-04
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Able to consent and agree to participate in the project after discussing the project
- Coming to The Everett Clinic during the operational project duration
- Evidence of upper respiratory symptoms suggesting higher risk of testing positive for SARS-CoV-2 virus.
You may not qualify if…
- Not able to demonstrate understanding of the study
- Not willing to commit to having all four samples collected
- Medical history evidencing any of the following
- Active nosebleed in the past 24 hours
- Nasal surgery in the past two weeks
- Chemotherapy treatment with low platelet and low white blood cell counts
- Acute facial trauma
Where it is running
- Everett Clinic — Seattle, Washington, United States
Full record on ClinicalTrials.gov
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