Skip to content

Assesment of the Metabolomic Signature in COVID-19 Patients

Assesment of the Metabolomic Signature in COVID-19 Patients (SignCov Study)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04497272
Acronym
SignCov
Enrollment
150
Registered
2020-08-04
Start date
2020-08-07
Completion date
2022-07-31
Last updated
2022-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID 19

Brief summary

Metabolomics is the analysis of small molecules in a biological sample (cells, tissues or biological fluids). It can potentially detect very sensitively any change related to a pathology or exposure to a toxic agent. The analyses are fast, inexpensive and therefore applicable in routine, particularly in health care. Given the emergence of this new disease, COVID-19, there is a real need to better understand the pathophysiological mechanisms of SARS-CoV-2 infection. In this context, metabolomics could have a place and could lead to the development of interesting diagnostic or prognostic tools. The objective of this study is to identify, through the analysis of biological samples (blood and urine), whether there is a metabolomic signature in patients with COVID-19.

Interventions

OTHERCOVID-19 patients

It will consist in the collection of 1 additional tubes at their blood draw and 1 urine sample.

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Patient with COVID-19 disease

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patient over 18 years of age * affiliated to a social security scheme * consultant in the emergency department and/or being hospitalized for suspected SARS CoV infection * confirmation, after medical examination, of the need for a biological examination (this will negate the need for additional venipuncture)

Exclusion criteria

* Patient who do not meet inclusion criteria * Person subject to a guardianship order * Opposition to the use of the data or samples (withdrawal of non-opposition) / Sponsor's or investigator's decision

Design outcomes

Primary

MeasureTime frameDescription
Identifying the metabolomic signatureEnrollmentTo dentified a metabolomic profile using liquid chromatography combined with mass spectrometry (LC-MS) on the serum and urine of COVID-19 patients

Secondary

MeasureTime frameDescription
Identification of the metabolomic profile according to clinical severity.EnrollmentIdentification of the metabolomic profile of patients infected with SARS CoV 2 in the following subgroups: pauci-symptomatic patients, symptomatic patients without clinical severity criteria, and critically ill COVID-19 patients.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026