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Environmental Factors Associated With Peripheral Neuropathies in French Guiana

Environmental Factors Associated With Peripheral Neuropathies in French Guiana

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07341997
Acronym
YANANER
Enrollment
78
Registered
2026-01-15
Start date
2025-12-08
Completion date
2027-07-31
Last updated
2026-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bita, Environmental Risk Factor, Lead Neuropathy, Mercury Neuropathy, Peripheral Neuropathies

Keywords

Preipheral neuropathies, French guiana, Mercury, Lead, Arboviruses, Environment

Brief summary

Peripheral neuropathies (PN) affect 1% of the global population, particularly the elderly. About 20-30% of cases remain unexplained. In French Guiana, we hypothesize that factors like neurotoxic traditional plant remedies, arboviral disease outbreaks, and mercury exposure from illegal gold mining may contribute to PN. The study aims to assess the association between PN and exposure to arboviral infections, heavy metals, and plant consumption in French Guiana.

Detailed description

Peripheral neuropathies (PN) affect 1% of the global population, with higher prevalence in the elderly. They lead to gait disorders and chronic pain, severely impacting quality of life. Despite thorough investigations, 20-30% of cases have no identified cause. In French Guiana, unique factors may contribute to these neuropathies, including the use of potentially neurotoxic traditional plant remedies and outbreaks of arboviral diseases, which can complicate conditions like Guillain-Barré syndrome. Additionally, illegal gold mining exposes residents to mercury, both directly and through environmental contamination. We hypothesize that these local factors might explain the unidentified cases of PN and exacerbate neuropathies in patients with pre-existing nerve vulnerability, such as diabetic neuropathy. This is a prospective multicenter case-control study being conducted in hospitals in Cayenne and Saint-Laurent du Maroni. At the inclusion visit, blood samples will be taken to assess arbovirus serology, particularly for Zika, Chikungunya and Dengue, as well as to measure levels of heavy metals, including mercury and lead. In addition, urine and hair samples will be taken to analyze these heavy metals. Participants will also fill in a questionnaire about their plant consumption. They will not be followed as part of the research.

Interventions

Patients diagnosed with diabetic peripheral neuropathy or chronic idiopathic axonal polyneuropathy.

Sponsors

Admin CIC
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

This is a prospective multicenter case-control study being conducted in hospitals in Cayenne and Saint-Laurent du Maroni. At the inclusion visit, blood samples will be taken to assess arbovirus serology, particularly for Zika, Chikungunya and Dengue, as well as to measure levels of heavy metals, including mercury and lead. In addition, urine and hair samples will be taken to analyze these heavy metals. Participants will also fill in a questionnaire about their plant consumption.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* For the Case group: patients diagnosed with diabetic peripheral neuropathy or chronic idiopathic axonal polyneuropathy * For the Control group: patients hospitalized or consulting at the hospitals in Cayenne and Saint-Laurent du Maroni, without peripheral neuropathy.

Exclusion criteria

* For the Case and Control groups: patients under the age of 18, those who object to participation and those who are unable to complete the questionnaire.

Design outcomes

Primary

MeasureTime frameDescription
Comparison of exposure rates among cases and controlsAt inclusionThe primary endpoint will be the comparison of rates of exposure to arboviruses, heavy metals and consumption of potentially neurotoxic plants in cases and controls. The heavy metals assay and the questionnaire will be carried out at the inclusion visit.

Secondary

MeasureTime frameDescription
Peripheral Nerve Disability (PND) determinationAt inclusionSecondary endpoint will be determination of Peripheral Nerve Disability (PND)
Genetic mutations indentificationAt inclusionSecondary endpoint will be identification of genetic mutations responsible for peripheral neuropathy

Countries

French Guiana

Contacts

Primary ContactNathalie DESCHAMPS, Principal Investigator
nathalie.deschamps@ch-cayenne.fr+594 594 397 317
Backup ContactVincent De Paul SENEKIAN, Principal Investigator
v.senekian@ch-ouestguyane.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026