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Scientists hunt for clues to deadly Mosquito-Borne viruses
NCT ID NCT07119086
First seen Sep 15, 2026 · Last updated Sep 16, 2026 · Updated 1 time
Summary
Researchers are studying people in Réunion and Mayotte who seek care for dengue, chikungunya, or Zika to understand why some cases become severe. The study collects blood and urine samples and asks patients about their quality of life. By comparing clinical, demographic, and environmental factors, the team aims to build risk profiles that could help doctors predict who needs urgent care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If researchers identify which patients face the highest risk of severe arbovirus illness, doctors could target monitoring and prevention more effectively in outbreak regions.
- What could go wrong
- This observational study cannot prove cause and effect, and its findings may not apply to other regions with different viruses, climates, or healthcare systems.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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May 2037
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
1st case : Inclusion Criteria: * Adult, child or newborn \> 2.5kg on day of inclusion. * Use of one of the hospital departments participating in the research, in an emergency room, full hospitalization, day hospitalization or outpatient clinic. * Suspected, probable or biologically confirmed arbovirosis: A suspected case of arbovirosis is defined as : * asymptomatic contact case of a patient with probable or confirmed arbovirosis * symptomatic or non-symptomatic newborns of mothers who were viremic for arbovirosis during pregnancy, or who had probable or confirmed arbovirosis during pregnancy. * In a patient with a history of a stay in an arbovirus circulation zone in the 2 weeks prior to consultation (for imported cases only). * In a patient with compatible clinical symptoms during the epidemic period A probable case of arbovirosis is defined by : * the association of at least 2 objectified or reported signs or biology suggestive of arbovirosis: fever (reported by the patient or family, or documented), headache, rash, myalgias, arthralgias, abdominal pain, bleeding, thrombocytopenia, or * for children under 6: by the reporting (by the family or documented) of a fever on the day of inclusion or in the preceding 7 days, possibly accompanied by pain. A biologically confirmed case of arbovirosis is defined by : \- A positive plasma RT-PCR or urine RT-PCR (Zika virus) Case 2 : - Retrospectively, patients with sufficiently documented definite, probable or suspected arbovirosis, who give oral consent for their data to be collected retrospectively and/or to continue the study follow-up. Exclusion Criteria: 1\. Patient ou titulaire de l'autorité parentale non affiliés ou non bénéficiaires d'un régime de sécurité sociale.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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PRCT
RECRUITINGSaint-Pierre, France