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NCT Number: NCT07611994

Analysis of Chlordecone Tissue Concentrations in Patients Treated for Thyroid Surgery at Guadeloupe University Hospital

Chlordecone, an organochlorine pesticide used in the French Caribbean for several decades, is recognized as an endocrine disruptor. Accumulation in thyroid tissue may be modeled using several factors, including blood chlordecone levels, environmental exposure associated with place of residence, and dietary habits.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU de la Guadeloupe

Les Abymes, 97159, Guadeloupe

Location contact

suzy Duflo, MD PhD

CONTACT

[email protected]

About this study

Chlordecone, an organochlorine pesticide, is recognized as an endocrine disruptor. Following ingestion, this molecule is preferentially stored in the liver and, to a lesser extent, in adipose tissue. The development of thyroid goiter may be promoted by exposure to certain substances. Environmental pollutants have been shown to increase TSH secretion, and prolonged exposure to endocrine disruptors affecting the pituitary-thyroid axis has been associated with thyroid neoplasia.

Currently, exposure to chlordecone is assessed through measurement of chlordeconemia (plasma concentration), reflecting exposure during the months preceding sampling and providing an estimate of body burden at the time of assessment. However, chlordecone impregnation in thyroid tissue and adjacent structures has not yet been investigated in humans.

The aim of this study is to model chlordecone concentration in tissues using chlordeconemia, occupational activity, dietary habits, and place of residence.

A biological collection will be established and stored at the Biological Resources Center (CRB) of the University Hospital to support the primary and secondary objectives. Blood, adipose tissue, and thyroid tissue samples will be collected.

The inclusion period will last 11 months, each participant will be involved for 4 months, and the total study duration will be 16 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • adult patients hospitalized at the Guadeloupe University Hospital for surgical treatment of thyroid pathology
  • person affiliated to or beneficiaries of a social security system
  • person with free, informed, and written consent signed by the participant and the investigator

Exclusion criteria

  • patients subject to a judicial safeguard measure,
  • patient under 18 years old
  • patient without signed consent
  • current pregnancy at the time of inclusion

Treatment and study plan

Blood and thyroid tissue collection

Other

Collection of blood, thyroid tissue, and adjacent adipose tissue samples during routine thyroid surgery for measurement of chlordecone concentration and assessment of exposure-related factors.

Primary outcomes

  1. chlordecone concentration in the adipose tissue adjacent to the thyroid

    Time frame: During surgery

    Chlordecone concentration measured in adipose tissue adjacent to the thyroid collected during thyroid surgery.

  2. Chlordecone concentration in blood

    Time frame: 1 day before surgery

    Chlordecone concentration measured in blood samples collected one day before surgery.

Secondary outcomes

  1. Occupational exposure category

    Time frame: At enrollment

    Occupational activity classified as high or low potential exposure to chlordecone based on professional activity collected through a self-administered questionnaire. Agricultural workers and livestock breeders will be classified as high exposure occupations

  2. Residential environmental exposure assessment

    Time frame: At enrollment

    Environmental exposure assessment based on residential history during the previous 10 years. Residential addresses reported for periods longer than 3 months will be geolocated and linked to soil contamination maps established by CIRAD.

  3. Dietary exposure assessment

    Time frame: At enrollment

    Dietary habits assessed using a self-administered questionnaire collecting information on food consumption patterns and food origin.

Study contacts

Contact information is provided by the study sponsor or research team.

mélanie petapermal, Master degree

CONTACT

[email protected]

+590590934667 ext. +590

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de la Guadeloupe

Other

Collaborators

  • Institut Pasteur de Guadeloupe

Registry information

Acronym: COTICHLO

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
May 28, 2026
Registry last updated
Jun 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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