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COVID-19 Seroprevalence Study in French Guiana

COVID-19 Seroprevalence Study in French Guiana

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04490850
Acronym
EPI-COVID-POP
Enrollment
3541
Registered
2020-07-29
Start date
2020-07-15
Completion date
2021-09-24
Last updated
2022-02-15

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

Conditions

Coronavirus Infection, Covid19, SARS-CoV Infection, Severe Acute Respiratory Syndrome

Keywords

SARS-CoV-2, COVID-19, Serology, French Guiana

Brief summary

Serological surveys measuring anti-severe acute respiratory syndrome coronavirus 2 (anti-SARS-CoV-2) antibodies in the population to assess the extent of the infection and the COVID-19 immunity of the population in French Guiana.

Detailed description

Serological surveys measuring anti-severe acute respiratory syndrome coronavirus 2 (anti-SARS-CoV-2) antibodies in the population to assess the extent of the infection and the COVID-19 immunity of the population in French Guiana. This study is a interventional study that present minimal risks and constraints. The results of the study will allow estimation of COVID-19 virus infection, severity and attack rates, as well as inform public health responses and policy decisions in the French Guiana territory.

Interventions

PROCEDUREBlood sample

Blood sample

Sponsors

Institut Pasteur de la Guyane
CollaboratorUNKNOWN
Laboratoire de biologie médicale, Institut Pasteur de la Guyane
CollaboratorUNKNOWN
Laboratoire de biologie médicale de Kourou, French Guiana
CollaboratorUNKNOWN
Laboratoire de biologie médicale du Centre hospitalier de Saint-Laurent du Maroni, French Guiana
CollaboratorUNKNOWN
Eurofins
CollaboratorINDUSTRY
Centres Délocalisés de Prévention et de Soins, Centre Hospitalier Andrée Rosemon de Cayenne, Frech Guiana
CollaboratorUNKNOWN
Institut Pasteur
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Person going to a prevention and care center or medical biology analysis laboratory as part of the care, regardless age, regardless of an acute or previous infection with COVID-19; * State of health compatible with a blood sample as defined in the protocol

Exclusion criteria

* Inability to consent * Person under guardianship or curatorship * Known pathology or a health problem contraindicated with the collect of blood sample.

Design outcomes

Primary

MeasureTime frameDescription
Measure of the COVID-19 immunity of the population1 yearThe COVID-19 immunity of the population will be assessed by evaluating the anti-severe acute respiratory syndrome coronavirus 2 (anti-SARS-CoV-2) antibodies

Secondary

MeasureTime frameDescription
Evaluation of the level of asymptomatic and pauci-symptomatic infections1 yearThe proportion of asymptomatic and pauci-symptomatic infections will be measured in the population

Countries

French Guiana

Outcome results

None listed

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