NCT04954352

Brief Summary

A local network is being set up to study the impact of arboviruses in our region. It is committed to a one-health approach, in particular with research without a priori for new viruses hosted among vectors and wildlife. The candidates identified by high throughput sequencing approaches will serve as a basis for the development of serological and molecular tools for their detections. These tools will be used to assess the possible circulation of these new viruses in humans in biological collections created within the framework of this project Arbodocc .

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
400

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2020

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

July 5, 2021

Completed
3 days until next milestone

First Posted

Study publicly available on registry

July 8, 2021

Completed
3.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 20, 2024

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2024

Completed
Last Updated

July 8, 2021

Status Verified

July 1, 2021

Enrollment Period

5 years

First QC Date

July 5, 2021

Last Update Submit

July 5, 2021

Conditions

Keywords

Patients with arboviral infection compatible signsUnexplained isolated feverNeurological infection conditions without any identified etiologyArbovirusArboviral like infectious disease

Outcome Measures

Primary Outcomes (1)

  • Seroprevalence

    Detection of antibodies targeting specific antigens of newly identified arboviruses

    1 day

Secondary Outcomes (1)

  • Molecular detection

    1 day

Eligibility Criteria

AgeUp to 80 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

* Patients admitted at the Monpellier University Hospital for any infectious syndrome compatible with an arboviral infection * Healthy volunteers for seroprevalence investigation

You may qualify if:

  • \- Patients admitted at the Monpellier University Hospital for any infectious syndrome compatible with an arboviral infection with samples available

You may not qualify if:

  • \- Informed consent non obtain for samples used

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Uh Montpellier

Montpellier, 34295, France

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Blood and CSF samples

MeSH Terms

Conditions

Arbovirus InfectionsSevere Acute Respiratory Syndrome

Condition Hierarchy (Ancestors)

Vector Borne DiseasesInfectionsVirus DiseasesRespiratory Tract InfectionsCoronavirus InfectionsCoronaviridae InfectionsNidovirales InfectionsRNA Virus InfectionsRespiratory Tract Diseases

Study Officials

  • Vincent Foulongne, PhD

    UH MONTPELLIER

    STUDY DIRECTOR

Central Study Contacts

Yannick Simonin, PhD

CONTACT

Vincent Foulongne, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 5, 2021

First Posted

July 8, 2021

Study Start

January 1, 2020

Primary Completion

December 20, 2024

Study Completion

December 30, 2024

Last Updated

July 8, 2021

Record last verified: 2021-07

Locations