Human Epidemiology of Newly Identified Arboviruses
ARBODOCC
Epidemiology in Humans of New Arbovirusus Sorted Out From Metagenomic Screen in Local Vectors and Animal Hosts.
1 other identifier
observational
400
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2020
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2020
CompletedFirst Submitted
Initial submission to the registry
July 5, 2021
CompletedFirst Posted
Study publicly available on registry
July 8, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2024
CompletedJuly 8, 2021
July 1, 2021
5 years
July 5, 2021
July 5, 2021
Conditions
Keywords
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
* 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
- University Hospital, Montpellierlead
- UMR ASTRE (CIRAD)collaborator
- Institut Pasteurcollaborator
- UMR PCCEIcollaborator
Study Sites (1)
Uh Montpellier
Montpellier, 34295, France
Biospecimen
Blood and CSF samples
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Vincent Foulongne, PhD
UH MONTPELLIER
Central Study Contacts
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