Actively Recruiting
Observational Study of Travellers Pathologies
Led by Institut Pasteur · Updated on 2025-05-01
11000
Participants Needed
1
Research Sites
625 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Traveling to emerging countries is associated with a significant risk of encountering health issues specific to the destination, such as gastrointestinal and respiratory infections, malaria episodes, and road traffic accidents.These conditions are associated with behavioral, geographical, or environmental risk factors. A better understanding of these factors will enable the development of targeted recommendations to minimize travel related health issues. The main objective of this study is to determine the incidence of pathologies occurring during travel outside the metropolitan territory.
CONDITIONS
Official Title
Observational Study of Travellers Pathologies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Owns a smartphone compatible with electronic data collection
- Preparing to travel outside mainland France
- Affiliated with or covered by Social Security or private insurance
- Willing to participate in the EOP study
- Consent to participate in the EOP-Arbo sub-study for blood sample collection (if applicable)
- Consent to participate in the EOP-AMR sub-study for fecal sample collection (if applicable)
You will not qualify if you...
- Travel duration of 3 days or less
- Travel duration longer than 12 months
- Traveling as part of expatriation without planned movement outside the settlement in the destination country
- Under legal protection or unable to give consent
- For EOP-Arbo sub-study: deemed unfit by investigator for blood sampling
- No specific exclusion criteria for EOP-AMR sub-study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Medical Center of Institut Pasteur
Paris, France, 75015
Actively Recruiting
Research Team
F
Fabien TAIEB, MD
CONTACT
J
Julia ABAD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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