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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02827175
Other study ID # 2013-45
Secondary ID 2013-A01536-39
Status Completed
Phase N/A
First received
Last updated
Start date January 7, 2014
Est. completion date October 26, 2022

Study information

Verified date April 2023
Source Assistance Publique Hopitaux De Marseille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Annually about 10 to 15 million international travelers from Europe visit tropical countries. Returning from a journey, fever is the cardinal symptom of many infections. This is the second reason for consultation (23%) for return from a trip, after digestive disorders (42%). Urgent evaluation must always be proposed. Although that may be the manifestation of a benign disease, fever of return can also presage a rapidly progressive and lethal disease. In 50% of cases, patients return home, after treatment and disappearance of symptoms, though the microorganism responsible for the pathology is not able to be identified. The prescription of a series of systematic biological examinations in the form of a diagnostic kit has shown its relevance and its effectiveness in improving the etiological diagnosis of endocarditis and pericardites for optimal support. In this study we propose to assess the effectiveness of the systematic prescription of a diagnostic kit 'fever of the traveler' to all patients hospitalized with a fever after returning from a trip. "Ready to use" kit brings together in a single bag (i) instructions for use, (ii) the tubes, bottles and jars for the etiological diagnosis of fever of the traveler in the usual support (iii) an additional blood tube for research of pathogens emerging. Primary: To assess the effectiveness of a diagnostic kit for the etiological diagnosis of fevers of travelers on the return. Hypothesis: Improvement of at least 15% of the etiological diagnosis of fevers of travelers on the return through the development of a diagnostic kit.


Recruitment information / eligibility

Status Completed
Enrollment 110
Est. completion date October 26, 2022
Est. primary completion date July 24, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient with a T >38.5 ° C with or without associated clinical signs. - Patient who traveled outside metropolitan France within 45 days with the hospitalization. - Patient is more than 18 years old. - Patient who accept to have his medical records reviewed for research. - Patient with health insurance Exclusion Criteria: - a feverish syndrome beyond 45 days after the return of their journey. - a clinical symptomatologie on the return to journey without associated fever, - minor(miner) ( 18 years). - Pregnant or breast-feeding woman. - Incapable major patient or outside state to express its consent.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
blood sample


Locations

Country Name City State
France Asssitance Publique Hopitaux de Marseille Marseille

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of etiological diagnosis established in relation to the number of prescribed kits 3 years