Surveillance of Summer Febrile Syndromes of Viral Origin in South of France

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-02-28

Study Completion Date

2011-07-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Summer Febrile Syndromes of Viral Origin

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Interventions

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BLOOD DRAW

specific interview, sequential blood collection to allow virus isolation, molecular and serological diagnostics in patients

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Old: equal to or higher than 5 years Living in the south of France, without voyage abroad in the 2 weeks preceding inclusion Presenting a fever or a syndrome pseudogripal since less than 7 days without diagnostic orientation nor infectious pathology of body,
* Affiliated with a mode of social security
* After obtaining free and informed of the written assent

Exclusion Criteria

* Subject whose adhesion with the protocol is improbable according to the investigator
* Expectant mother
* Subject taking part in another clinical trial or in period of exclusion of a preceding clinical trial infectious
* Pathology of body requiring a specific treatment
* Discovered after inclusion d' a pregnancy

Minimum Eligible Age

5 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No