NCT07611994

Brief Summary

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.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
69

participants targeted

Target at P50-P75 for not_applicable

Timeline
15mo left

Started Jul 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress7%
Jul 2026Nov 2027

First Submitted

Initial submission to the registry

May 21, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 28, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

July 1, 2026

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2027

Last Updated

June 1, 2026

Status Verified

May 1, 2026

Enrollment Period

1.3 years

First QC Date

May 21, 2026

Last Update Submit

May 28, 2026

Conditions

Keywords

chlordeconethyroid nodesthyroid disruptor

Outcome Measures

Primary Outcomes (2)

  • chlordecone concentration in the adipose tissue adjacent to the thyroid

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

    During surgery

  • Chlordecone concentration in blood

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

    1 day before surgery

Secondary Outcomes (3)

  • Occupational exposure category

    At enrollment

  • Residential environmental exposure assessment

    At enrollment

  • Dietary exposure assessment

    At enrollment

Study Arms (1)

Participants undergoing thyroid surgery

OTHER

Participants undergoing thyroid surgery with prospective collection of blood, thyroid tissue, and adjacent adipose tissue samples for chlordecone concentration assessment and evaluation of exposure-related factors.

Other: Blood and thyroid tissue collection

Interventions

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.

Participants undergoing thyroid surgery

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • patients subject to a judicial safeguard measure,
  • patient under 18 years old
  • patient without signed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU de la Guadeloupe

Les Abymes, 97159, Guadeloupe

Location

MeSH Terms

Conditions

Thyroid Diseases

Interventions

Blood Specimen Collection

Condition Hierarchy (Ancestors)

Endocrine System Diseases

Intervention Hierarchy (Ancestors)

Specimen HandlingClinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisPuncturesSurgical Procedures, OperativeInvestigative Techniques

Study Officials

  • suzy Duflo, MD PhD

    CHU de la Guadeloupe

    PRINCIPAL INVESTIGATOR

Central Study Contacts

mélanie petapermal, Master degree

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Model Details: Observational, analytical, single-center, cross-sectional study with prospective data collection.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 21, 2026

First Posted

May 28, 2026

Study Start

July 1, 2026

Primary Completion (Estimated)

November 1, 2027

Study Completion (Estimated)

November 1, 2027

Last Updated

June 1, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Locations