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OpenTrials
Completed

NCT Number: NCT05704803

COVID-19 Molecular OTC At Home Test

The objective of this study is to evaluate the a molecular, OTC/At-Home COVID-19 Test in individuals presenting at a medical facility. In eligible subjects, nasal samples will be collected for use with the at-home molecular COVID-19 Test, which will be compared to the Zymo® rRT-PCR test results obtained via samples specified by the sponsor (e.g., AN [anterior nares] swab) to determine accuracy of the at-home/OTC molecular COVID-19 Test in detecting COVID-19 in participants.

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Key information

Age range

2 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Bright Research Center, Miami, Florida, United States

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About this study

The molevular, at-home COVID-19 Test is a unique rapid molecular test system intended to detect SARS-CoV-2 virus in the OTC setting using a dedicated reusable test reader to test nasal swab samples. Early testing will help to determine limit of detection (LOD) of the molecular COVID-19 Test and will be compared to a sensitive molecular test that has been authorized for emergency use by the FDA. The COVID-19 Test will leverage the processing and testing of the associated Swab device when inserted directly into the reaction tube (Key) where reverse transcription, Loop-Mediated Isothermal DNA Amplifications (LAMP) processing and sequence-specific probe technologies to detect segments of the SARS-CoV-2 genome are managed automatically by the reusable test reader.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

All Participants must meet ALL of the following:

  • ≥ 2 years of age. Subjects ages 2 ≤ x ≤ 17 will provide assent in addition to parent / legal guardian's consent.
  • Able to read and write in English and/or Spanish (subjects or guardians)
  • Willing and able to provide informed consent (subject or Legally authorized Representative (LAR)). Subjects unable to consent will provide assent in addition to LAR consent.

Symptomatic Participants must meet BOTH of the following:

  • Have at least one of the following symptoms the day of the test:
  • Fever
  • Cough
  • Shortness of Breath
  • Difficulty Breathing
  • Muscle Pain
  • Headache
  • Sore Throat
  • Chills
  • New loss of taste or smell
  • Congestion
  • Runny nose
  • Onset of symptoms occurred within the past 7 calendar days.

Asymptomatic Participants must meet BOTH of the following:

  • Not experiencing any of the following symptoms at the time of specimen collection and testing: fever, cough, shortness of breath or difficulty breathing, new loss of taste or smell, muscle or body aches, headache, sore throat, congestion or runny nose, nausea or vomiting or diarrhea.
  • Exposed to known COVID-19 positive individuals or are suspected to have had COVID-19 over the past 7 calendar days.

Exclusion criteria

Participants must not meet ANY of the following:

  • Eating or drinking 30 minutes prior, or smoking 60 minutes prior to specimen collection.
  • Unable to tolerate sample collection, or has contraindications to collection such as nasal bleeding, ulcers, or surgery within the past 3 months.
  • Underwent a nasal wash / aspirate as part of standard of care < 24 hours prior to the study start.
  • Currently receiving or has received within the past 30 days of the study visit an experimental drug, biologic, or device including treatment or therapy.
  • Previously participated in this study.

Treatment and study plan

Diagnostic Test: IN Vitro

Diagnostic Test

In vitro diagnostic test for COVID-19 using anterior nasal swabs.

Primary outcomes

  1. Correlation of the 3EO Health SARS-CoV-2 standard of care (PCR) Zymo rRT-PCR results of the anterior nare sample.

    Time frame: 1-16 weeks

    The primary endpoints of this study will be the correlation of the 3EO Health SARS-CoV-2 OTC At Home Test results from nasal samples to the comparator, standard of care (PCR) Zymo rRT-PCR results of the anterior nare sample

Sponsors and collaborators

Lead sponsor

3EO Health

Industry

Registry information

Official study title

Prospective, Multi-Center, Non-Randomized Study to Evaluate OTC At Home SARS-CoV-2 Molecular Diagnostic Test

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jan 30, 2023
Registry last updated
Sep 28, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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