ClinicalTrials.gg
Status unknownNCT03378882ACCRAGUpdated Dec 11, 2020

Research for Angiostrongylus Cantonensis and Costaricensis in French West Indies and French Guiana

An observational study in Angiostrongylosis and Hypereosinophilia, sponsored by University Hospital Center of Martinique. Status unknown at 1 site in France. Per ClinicalTrials.gov, last updated 2020-12-11.

Sponsored by University Hospital Center of Martinique · Observational

The sponsor has not verified this record recently (last verified Dec 2020), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
20
Sex
All
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Study summary

Hospitals in the French West Indies (Fort-de-France (Martinique); Basse-Terre and Pointe-à-Pitre (Guadeloupe); and French Guiana (Cayenne, Saint-Laurent du Maroni)) have noted the emergence of eosinophilic meningitis cases in recent years. This finding is part os eosinophilic meningitis cases emergence and meningoencephalitis caused by the parasite Angiostrongylus cantonensis on the American continent and in the Greater Antilles.

In 2013, the investigation of an eosinophilic meningitis case by the Basse-Terre hospital team with a positive specific PCR in the CSF (CDC, Atlanta, USA) showed the first case of neuromeningeal angiostrongylosis in Guadeloupe. A similar case was diagnosed by serology at Pointe-à-Pitre University Hospital a few years earlier without having been published, and another serious case diagnosed also at Pointe-à-Pitre University Hospital Center in January 2017. The team at the Martinique University Hospital Center also reported several cases of eosinophilic meningitis with positive serologies for A. cantonensis carried out in laboratories outside Martinique (Laboratory of Parasitology, Gonesse, France; Thailand; and Tropical Institute and Public Health, Switzerland) in recent years.

The emergence of this parasitosis is related to the introduction of the intermediate host Achatina fulica on the American continent and the geographical evolution of the angiostrongylosis cases is intrinsically linked to that of the Achatins. To date, only two studies report the environmental presence of Angiostrongylus cantonensis in the Lesser Antilles. One proved the presence in rats (23.4%) on the island of Grenada, and the other in Guadeloupe, showing that 32.4% of Achatina fulica collected carried the parasite by specific PCR. In Martinique, where the number of cases is increasing, and in French Guiana, where there is an increase in the number of cases in neighboring countries, especially Brazil, no study has been conducted on this parasite.

In parallel with this finding, several serious digestive tables associated with strong hypereosinophilia were reported in Martinique and Guadeloupe in the 90s but also in recent years, the last case in December 2016. Etiological diagnoses were established by the discovery of Angiostrongylus costaricensis parasite in ileal pathological specimens. However, these cases could never be investigated by serology or specific PCR due to lack of diagnostic tools available in the French West Indies and Guiana region, and more broadly in metropolitan France.

Read the detailed description

Angiostrongylosis is a parasitosis caused by the nematode Angiostrongylus sp. The adult parasite lives in the rat's arteries (Rattus norvegicus and Rattus rattus), its definitive host, where it breeds. Stage 1 immature larvae are released into the environment in rat droppings. Stage 3 larval maturation, which is essential for the re-contamination of final hosts, is mainly carried out in the Buyina fulica mollusc (common name: Achatine).

The mode of contamination in humans is by ingestion of stage 3 parasitic larvae according to various modes: accidental ingestion of molluscs or salads soiled by "molluscan slime" (example: by consumption of salad, vegetables, non-washed fruits), voluntary ingestion of molluscs, manipulation of molluscs (children or fishermen), use of drinking water drawn from natural and non-disinfected water bodies. Hand-carried transmission after handling of Achatines is most often reported in young children.

In humans, these larvae have a different preferential tropism depending on the species of Angiostrongylus. The two main pathogenic species for humans are Angiostrongylus cantonensis and Angiostrongylus costaricensis.

Angiostrongylus cantonensis:

After ingestion by man, the larvae of Angiostrongylus cantonensis migrate to the central nervous system. They cause eosinophilic angiostrongyl meningitis and meningoencephalitis, which can lead to severe neurological sequelae (paralysis) or even death.

These clinical features are associated with eosinophilic pleocytosis in CSF (eosinophilic meningitis) and blood eosinophilia.

Angiostrongylus cantonensis was first described in Canton, China in 1935. To date, it is present in the Pacific Islands, Australia, Africa and recently on the American continent.

Angiostrongylus costaricensis:

After ingestion, the larvae of Angiostrongylus costaricensis migrate intestines and into the abdominal cavity. They cause severe abdominal pain mimicking those of appendicitis, haemorrhage and perforation digestive that can lead to death (2 to 8% of cases).

A major eosinophilia usually accompanies these unspecific clinical pictures. Angiostrongylus costaricensis does not have the same geographical distribution as Angiostrongylus cantonensis. It was first described in Costa Rica in 1967 and is endemic on the American continent, where it is at the origin of many human cases.

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Conditions studied

  • Angiostrongylosis
  • Hypereosinophilia

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Keywords

  • Angiostrongylosis
  • Hypereosinophilia
  • Eosinophilic meningitis
  • Meningoencephalitis
  • Achatina fulica
  • Angiostrongylus cantonensis
  • Angiostrongylus costaricensis
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In context

Eosinophilia

52 studies on the registry are indexed under Eosinophilia; 9 are open to participants now.

This study's planned enrollment of 20 is below the median of 86 across 18 observational studies indexed under Eosinophilia.

Browse Eosinophilia studies →

Lead sponsor

University Hospital Center of Martinique is the lead sponsor of 79 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All hospitalized patients, whatever their age, sex, weight, presenting hypereosinophilia.

Suspicious cases may come from different hospital services (pediatrics, infectiology, resuscitation, neurology, emergencies, ...).

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Hypereosinophilia associated with a meningeal table (= suspicion of neuromeningeal angiostrongylosis), or,
  • Hypereosinophilia associated with a severe gastrointestinal table(= suspicion of intestinal angiostrongylosis)

Exclusion criteria

Exclusion Criteria:

  • Refusal of the patient to be included in the study
  • Angiostrongylosis of importation (contracted outside the French West Indies - French Guiana region)
  • Absence of hypereosinophilia
  • Hypereosinophilia in the context of an other parasitosis
  • Non-parasitic hypereosinophilia
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
20 participants (estimated)
Patient registry
No

Interventions

  • BiologicalParasitic serologies

    Suspected angiostrongylosis - Angiostrongylus cantonensis: * An aliquot of CSF and an aliquot of serum will be sent to the laboratory of tropical medicine in Switzerland for research of specific antibodies. * A CSF aliquot will be sent to the CDC for PCR. Suspected angiostrongylosis- Angiostrongylus costaricensis: - An aliquot of serum will be sent to the laboratory of tropical medicine in Switzerland for research of specific antibodies.

  • ProcedureBiopsy

    Suspected angiostrongylosis - Angiostrongylus costaricensis: - A piece of biopsy or intestinal resection will be sent to the pathology laboratory for parasitic elements suggestive of Angiostrongylus costaricensis infection

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What researchers measure

Primary outcomes

  1. Number of participants with angiostrongylosis A. cantonensis

    The crude incidence will be calculated: Reported number of cases of angiostrongylosis A. cantonensis diagnosed during the study inclusion period (3 years) on the total population (population census data). The number of human cases of angiostrongylosis A. cantonensis diagnosed since the emergence of the parasite in the West Indies and Guiana will be calculated. The standardized incidence (on age and sex) of this infection will be calculated.

    Time frame: 36 months

  2. Number of participants with angiostrongylosis A. costaricensis

    The crude incidence will be calculated: Reported number of cases of angiostrongylosis A. costaricensis diagnosed during the study inclusion period (3 years) on the total population (population census data). The number of human cases of angiostrongylosis A. costaricensis diagnosed since the emergence of the parasite in the West Indies and Guiana will be calculated. The standardized incidence (on age and sex) of this infection will be calculated.

    Time frame: 36 months

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Study locations

1 of 1 sites recruiting
  • CHU of Martinique
    Fort-de-France, 97261, France
    Recruiting
    • Nicole DESBOIS, MD · Contact
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Apr 2018 (actual). Primary completion is estimated for Apr 2021, 36 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 7, 2017
First posted
Dec 20, 2017
StartActual
Apr 3, 2018
Primary completionEst.
Apr 3, 2021
CompletionEst.
Aug 1, 2021
Last update
Dec 11, 2020
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 11, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03378882
Lead sponsor
University Hospital Center of Martinique
Collaborators
University Hospital Center of Pointe-à-Pitre/Abymes (Guadeloupe), Hospital Center of Basse-Terre (Guadeloupe), Hospital Center of Cayenne (French Guiana), Hospital Center of Saint-Laurent du Maroni (French Guiana)
Responsible party
Sponsor
First posted
Dec 20, 2017
Start date
Apr 3, 2018
Primary completion
Apr 3, 2021 (estimated)
Completion
Aug 1, 2021 (estimated)
Last update
Dec 11, 2020

Study contacts

Nicole DESBOIS, MD
Contact
nicole.desbois-nogard@chu-martinique.fr
0596559665 ext. +33
Céline DARD, MD
Contact
cdard@chu-grenoble.fr
Nicole DESBOIS, MD
principal investigator · CHU of Martinique

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2020. You cannot join it, but the record below documents what was studied.

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