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Not yet recruiting NCT07611994

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

No phase Interventional Thyroid and Parathyroid Surgery

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Blood and thyroid tissue collection.
Who it may be relevant to
Registry conditions: Thyroid and Parathyroid Surgery. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Guadeloupe
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Detailed description

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.

Interventions

  • Other Blood and thyroid tissue collection
    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 outcome measures

  • chlordecone concentration in the adipose tissue adjacent to the thyroid [Time frame: During surgery]
  • Chlordecone concentration in blood [Time frame: 1 day before surgery]
Secondary outcome measures (3)
  • Occupational exposure category [Time frame: At enrollment]
  • Residential environmental exposure assessment [Time frame: At enrollment]
  • Dietary exposure assessment [Time frame: At enrollment]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Basic science

Study locations

Guadeloupe · 1 center
  • CHU de la Guadeloupe — Les Abymes

Identifiers

NCT: NCT07611994 · PAP_RIPH2_2025/08

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗