ClinicalTrials.Veeva

Menu

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

P

Public Assistance-Hospitals of Marseille (AP-HM)

Status

Completed

Conditions

Summer Febrile Syndromes of Viral Origin

Treatments

Other: BLOOD DRAW

Study type

Interventional

Funder types

Other

Identifiers

NCT00842166
2008 19
2008-A00793-52

Details and patient eligibility

About

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.

Enrollment

90 patients

Sex

All

Ages

5+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems