Surveillance of Summer Febrile Syndromes of Viral Origin in South of France
2 other identifiers
interventional
90
1 country
1
Brief Summary
The aim is to document viral etiologies of isolated fevers and inlfuenza-like syndromes during summertime in South of France in order to better understand the role of known vector-borne viruses such as Toscana virus, West Nile virus during seasonal activity of the arthropod vector. In each of the four cities, a network of general practitioners will be associated in the project to recruit patients who are not hospitalized. The combined involvement of infectious disease specialists and general practitioner will augment the range of patients (mild disease and sever cases) in the study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2009
Typical duration for not_applicable
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
February 1, 2009
CompletedFirst Submitted
Initial submission to the registry
February 11, 2009
CompletedFirst Posted
Study publicly available on registry
February 12, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2011
CompletedAugust 29, 2014
August 1, 2014
2.4 years
February 11, 2009
August 28, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
to document viral etiologies of isolated fevers and inlfuenza-like syndromes during summertime in South of France
3 years
Secondary Outcomes (1)
Identification and characterization of emergent viruses responsible for estival fever in the south of France
3years
Interventions
specific interview, sequential blood collection to allow virus isolation, molecular and serological diagnostics in patients
Eligibility Criteria
You may qualify if:
- Affiliated with a mode of social security
- After obtaining free and informed of the written assent
You may not qualify if:
- Subject whose adhesion with the protocol is improbable according to the investigator
- Expectant mother
- Pathology of body requiring a specific treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Service des Maladies Infectieuses et Tropicales de l'Hôpital Nord, AP-HM
Marseille, France
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
REMI CHARREL
Assistance Publique Hopitaux De Marseille
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 11, 2009
First Posted
February 12, 2009
Study Start
February 1, 2009
Primary Completion
July 1, 2011
Study Completion
July 1, 2011
Last Updated
August 29, 2014
Record last verified: 2014-08