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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04614883
Other study ID # 2020_0143
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 21, 2020
Est. completion date February 26, 2021

Study information

Verified date June 2021
Source Hopital Foch
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In the context of the actual pandemia of the Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which requires a better diagnostic strategy for the management of patients. The study of volatile organic compounds (VOC) detected in exhaled air or in sweat, is an innovative research area for respiratory diseases. The analysis of VOC can be done either by the technique of the mass spectrometry which allows the identification of each VOC in the exhaled air or by the technique of electronic nose, simpler and faster, which provides an idea of the general profile of the VOC without identifying them. The VOC have shown their interest in some situations, such as diagnostic or prognostic tool in patients followed for thoracic tumorous pathology or bronchial or pulmonary vascular diseases. Moreover, it has recently been shown that properly trained dogs would be able to detect an olfactory signature of SARS-CoV-2 infection with a specificity greater than 90%; this olfactory signature corresponds to VOCs detectable by the flair of dogs (Nosaïs-Covid19 study). Validation of the diagnostic value of VOC analyzes by non-invasive and rapid methods (electronic nose analysis or mass spectrometry; detection by the scent of dogs) for the rapid detection and early diagnosis of a SARS-CoV-2 infection warrants the performance of this clinical study.


Recruitment information / eligibility

Status Completed
Enrollment 130
Est. completion date February 26, 2021
Est. primary completion date February 26, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Patients - Patents anaged at the Foch Hospital for suspected COVID-19 and any other patient whose management requires diagnosis of SARS-CoV-2 infection - Patients aged 18 or over; - Patients Fluent in French ; - Patients with a signed consent form; - Patients with a health insurance plan. 2. Healthy volunteers - Foch Hospital staff asymptomatic for SARS-CoV-2 infection; - Aged 18 yor over; - Fluent in french; - with a signed consent form; - With a health insurance plan. Exclusion Criteria: - Pregnant woman - Patient deprived of liberty by judicial or administrative decision

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Volatile Organic Compounds analysis
VOC analysis in exhaled air with e-noses and mass spectrometry. VOC analysis in sweat with mass spectrometry.
Other:
Canine odor detection of Volatile Organic Compounds
VOC analysis in sweat by trained dogs.

Locations

Country Name City State
France Foch hospital Suresnes

Sponsors (1)

Lead Sponsor Collaborator
Hopital Foch

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Validate the interest of VOCs analyzed by electronic noses and / or mass spectrometry for the diagnosis of a COVID-19 infection Comparison of variation of Volatile Organic Compound (VOC) profiles in exhaled air of patients between patients with symptoms suggestive of COVID and infection confirmed by Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) and those whose infection is ruled out based on the negativity of RT-PCR and clinical data 1 day
Secondary Identify the nature of VOCs associated with infection by SARS-CoV-2 by mass spectrometry in exhaled air and in sweat The equivalences and differences in nature of VOCs associated with infection with SARS-CoV-2 between exhaled air and sweat. 1 day
Secondary Assessment of the specificity and sensitivity of canine olfactory detection of COVs associated with infection by SARS-CoV-2 (COVID-19) Proportion of success in detecting samples from patients with symptoms suggestive of COVID and infection confirmed by PCR. 1 day
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