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COVID-19 Biological Samples Collection

Biological Samples Collection From Patients and Caregivers Treated at Bordeaux University Hospital for Asymptomatic and Symptomatic Severe Acute Respiratory Syndrome CoronaVirus 2 (SARS-CoV-2) Infection (COVID-19).

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04332016
Acronym
COLCOV19-BX
Enrollment
615
Registered
2020-04-02
Start date
2020-04-02
Completion date
2021-09-29
Last updated
2026-06-11

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

Conditions

Infection Viral

Keywords

COVID-19, SARS-CoV-2, coronavirus, biological samples

Brief summary

The coronavirus disease 2019 (COVID-19) outbreak is now considered as a public health emergency of international concern by the World Health Organization. In the context of the health emergency, research on the pathogen (the SARS-CoV-2 coronavirus), the disease and the therapeutic care is being organized. Research projects require the use of biological samples. This study aims at setting up a collection of biological samples intended for application projects in any discipline. The main objective of the study is to collect, process and store biological samples from patients and caregivers infected with SARS-CoV-2 (COVID-19) at the biological ressources center of the Bordeaux University Hospital.

Interventions

collection of whole blood samples, urine and stool samples, upper respiratory samples, post-mortem biopsies

Sponsors

University Hospital, Bordeaux
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 100 Years
Healthy volunteers
No

Inclusion criteria

* Patients / caregivers treated at Bordeaux University Hospital for asymptomatic or symptomatic infection by SARS -CoV-2 * men and women, adults and minors as well as pregnant or breastfeeding women * patients who died following infection with SARS-CoV-2 (specific criterion for post-mortem biopsies) * Be affiliated with or beneficiary of a social security scheme * Free and informed consent obtained and signed by the patient

Exclusion criteria

* Under guardianship or curatorship

Design outcomes

Primary

MeasureTime frameDescription
COVID-19 desease descriptionInclusion visit (Day 1)From blood samples: protein levels, whole genome sequence, transcriptomic analysis data. From upper respiratory samples: protein levels, virus transcriptomic analysis data. From stool: microbiota analysis data. From urine: protein level.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 12, 2026