Back to resultsSurveillance of Summer Febrile Syndromes of Viral Origin in South of France
Primary Purpose
Summer Febrile Syndromes of Viral Origin
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
BLOOD DRAW
Sponsored by
About this trial
This is an interventional prevention trial for Summer Febrile Syndromes of Viral Origin
Eligibility Criteria
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
Sites / Locations
- Service des Maladies Infectieuses et Tropicales de l'Hôpital Nord, AP-HM
Outcomes
Primary Outcome Measures
to document viral etiologies of isolated fevers and inlfuenza-like syndromes during summertime in South of France
Secondary Outcome Measures
Identification and characterization of emergent viruses responsible for estival fever in the south of France
Full Information
NCT ID
NCT00842166
First Posted
February 11, 2009
Last Updated
August 28, 2014
Sponsor
Assistance Publique Hopitaux De Marseille
1. Study Identification
Unique Protocol Identification Number
NCT00842166
Brief Title
Surveillance of Summer Febrile Syndromes of Viral Origin in South of France
Study Type
Interventional
2. Study Status
Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique Hopitaux De Marseille
4. Oversight
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Summer Febrile Syndromes of Viral Origin
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Other
Intervention Name(s)
BLOOD DRAW
Intervention Description
specific interview, sequential blood collection to allow virus isolation, molecular and serological diagnostics in patients
Primary Outcome Measure Information:
Title
to document viral etiologies of isolated fevers and inlfuenza-like syndromes during summertime in South of France
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Identification and characterization of emergent viruses responsible for estival fever in the south of France
Time Frame
3years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
REMI CHARREL
Organizational Affiliation
Assistance Publique Hopitaux De Marseille
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service des Maladies Infectieuses et Tropicales de l'Hôpital Nord, AP-HM
City
Marseille
Country
France
12. IPD Sharing Statement
Learn more about this trial
Surveillance of Summer Febrile Syndromes of Viral Origin in South of France
We'll reach out to this number within 24 hrs