Can a support program lower pesticide levels in guadeloupeans?
NCT ID NCT07251036
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study measures chlordecone (a pesticide) levels in the blood of 3000 adults in Guadeloupe. It also tests whether a multidisciplinary support program can help reduce those levels. Participants get free blood tests and personalized advice. The goal is to understand contamination and find ways to lower it.
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 successful, this could show that a support program helps lower chlordecone levels in the blood, pointing toward ways to reduce long-term exposure.
- What could go wrong
- This is an observational study, not a treatment trial. It may not prove the program directly causes lower levels, and results may not apply to other populations.
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 3,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2022
- Expected to finish
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Jun 2028
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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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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.
* All subject overs 18 years of age residing in Guadeloupe invited to participate to the program by the Regional Health Agency or subjects who requested a test from their doctor in the framework of the ministerial measure. * Subjects who have read the information note and signed the consent to participate in the study * Subjects with social security coverage Exclusion Criteria: * Refusal to participate * Person not affiliated with a social security scheme * Person under legal protection (safeguard of justice, guardianship, curatorship, etc.
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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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Centre Hospitalier Universitaire de la Guadeloupe
RECRUITINGPointe-à-Pitre, Guadeloupe, 97159, Guadeloupe