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NCT04760639 Clinical Trial

COVID Breath Test - Ancon

Covid19 Clinical Trial

Official title:
Breath Test Feasibility Trial for COVID-19 Infection Diagnosis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04760639
Other study ID # Pro00102970
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 16, 2020
Est. completion date September 20, 2022

Study information
Verified date November 2022
Source Medical University of South Carolina
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is designed to look at the effectiveness of a new technology call Nanotechnology Biomarker Tagging (NBT) in detecting COVID-19 infection using breath samples of patients. Participation in this study is expected to take less than one month and will consist of a breath sample being taken by the research team, a cheek swab being taken by the research team, a questionnaire that will be completed by the participant with the help of the research teams, and a review of your medical record.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date September 20, 2022
Est. primary completion date September 16, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 years and older - Patients that present for COVID-19 testing, have tested Covid negative, or Covid Positive patients. Exclusion Criteria: - Unable to consent - Patients on a ventilator - Pregnant Women

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Breath test
Participants provide a breath sample

Locations
Country Name City State
United States Medical University of South Carolina Charleston South Carolina

Sponsors (1)
Lead Sponsor Collaborator
Medical University of South Carolina

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Provide an adequate sample and compare the signals given from the two groups. The samples from the participants will be analyzed to identify the different signals given from Covid-19 positive patients and Covid-19 negative patients 10 minutes
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