Covid-19 Breath Test

  • STATUS
    Recruiting
  • participants needed
    250
  • sponsor
    Ancon Technologies Ltd
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Updated on 16 February 2024
See if I qualify
covid-19
discomfort

Summary

Can Nanotechnology Biomarker Tagging (NBT) be used to detect COVID-19 infection in people presenting for COVID-19 testing?

NBT can be used to detect the substances present in a person's breath. In this study the breath of people presenting for COVID-19 testing is going to be analysed. Analysing a large number of samples from people with COVID-19 (as confirmed by the standard swab test used by the NHS) will enable a breath profile to be produced, ie the substances present in the breath when someone has COVID-19. After the profile has been validated, NBT can be used to test whether or not a person has COVID-19 by seeing if their breath matches the profile.

Using this technology for COVID-19 testing has advantages over the current standard test. The sample can be analysed immediately in the clinical setting and the results are available in 5-10 minutes, so if the person tests negative they can go back to their normal life straight away. The current swab test takes around 72 hours for the results to be available, and the person needs to self-isolate during this time in case they test positive, resulting in potentially unnecessary days of work missed and inconvenience. The breath test is non-invasive and is unlikely to cause any discomfort, as the person is only required to breath normally into the device. This study will also review the practicalities of using this test. It is quick and easy to train people in how to carry out the test, so it could potentially easily be rolled out to testing sites.

Description

This is a Cohort Study which will collect non-invasive, expired breath sample, cheek swab and a Medical and Lifestyle questionnaire from participants.

When the participant presents for COVID-19 testing they will be asked to provide a cheek swab and breath sample, and complete the study questionnaire. They will not need to give any identifiable information or have a second visit. The samples will be analysed immediately and disposed of as clinical waste. ANCON will then use the data to build a breath profile of COVID-19 infection.

Sample and data collection method for inpatients:

  • Sequential (daily or every other day as able) breath and swab test will be taken from some of the patients admitted in the hospital (inpatients).
  • This will be taken from entry or start of the study to discharge or end of study or until patient or medical staff deem unsuitable to continue
  • This will enable to track infection and the relevant profile changes as covid-19 progresses and/or is treated. This will provide vital additional information around identifiers associated with the disease and its progress.

Anonymous Questionnaire - Each participant will be asked questions in the form of a short standard questionnaire based on:

  • Medical Information
  • Lifestyle Information

Details
Condition Covid-19 Infection
Age 16years - 100years
Treatment Breath Test & Cheek Swab
Clinical Study IdentifierNCT04459962
SponsorAncon Technologies Ltd
Last Modified on16 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

Male & Females
Age Above 16 years old
All Ethnicity
Any patients that come for COVID-19 testing
COVID Negative Patients (Further participants may be selected as control groups who have no current diagnosis of COVID-19.)
COVID Positive In-Patients

Exclusion Criteria

Outside of stated age range - below 16
Unable to consent
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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