Epidemiology and Genetics of the Amyotrophic Lateral Sclerosis in the French West Indies
NCT03367650 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70
Last updated 2017-12-11
Summary
The diagnosis and the follow-up of the patients reached of SLA is centralized, since a few years, at the the Caribbean Reference center of the rare neurological diseases (CERCA labélisé in 2006) in Martinique and at the Unity of coverage of the neuromuscular Diseases, SLA and the rare neurological diseases (create in 2010) in Guadeloupe. Several phenotypic characteristics seemed to us to take out again data collected during the follow-up of the patients (26 in Guadeloupe, since the creation of the unity) in particular patients' high proportion of exceptionally long evolution (more than 10 years). Besides, we diagnosed several cases (10 cases in Guadeloupe since 2000) of association SLA- Parkinsonien Syndrome.
This association, considered as exceptional could establish a particular phenotypic entity which we would like to describe. We are interested also originally geographical of the patients, with the hypothesis that he could exist in the Antilles one or several geographical isolates of the disease allowing to lead a étiologique investigation in search of a possible genetic or environmental cause.
Conditions
Interventions
- DIETARY_SUPPLEMENT
-
Blood sample and environmental survey
The intervention corresponds to a 10 ml of Blood sample and an environmental survey.
Sponsors & Collaborators
-
Centre Hospitalier Universitaire de la Guadeloupe
lead OTHER
Principal Investigators
-
Annie LANNUZEL, Professor, Neurological · Hospital University Center of Pointe-à-Pitre
Study Design
- Allocation
- NA
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-05-13
- Primary Completion
- 2020-05-13
- Completion
- 2023-05-13
Countries
- Guadeloupe
- Martinique
Study Locations
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