Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
150 participants
OBSERVATIONAL
2010-12-31
2018-08-31
Brief Summary
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The microscopic agglutination test (MAT) and culture are the reference standard test for diagnosis of leptospirosis, but they are only available in reference laboratories and their conclusive results requires convalescent sample or prolonged incubation. At present, only direct detection methods using PCR might provide rapid diagnosis during the early acute stage of the illness, when treatment is likely to have the greatest benefit.
Quantitative PCR also offers the ability to measure level of leptospiremia in clinical samples. Using qPCR based diagnosis, the investigators have the opportunity to study the association of level of leptospiremia and clinical manifestations in French West Indies. All qPCR-positive samples will be used for molecular typing.
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Detailed Description
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To determine if leptospiral bacterial load is associated with severe evolution of the disease (organ failure, internal bleeding, death) in French West Indies.
Secondary objective
1. To identify demographic, clinical, biological, bacteriological, and genetic factors (HLA) associated with severe complications of leptospirosis (organ failure, internal bleeding, death).
2. To identify demographic, clinical, biological, bacteriological, and genetic factors (HLA) associated with an altered quality of life after the acute phase of leptospirosis.
3. To collect human biological samples to allow studies of the individual susceptibility to the infection (genetic polymorphisms, HLA).
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Consulting a participating hospital center (emergency room, full hospitalization, day hospitalization, or outpatient visit).
* Diagnosis of leptospirosis confirmed by qPCR
* Possibility of follow-up throughout the 12-week study period.
* Patient registered in the French medical social security national program
* Acceptance to participate in the study and in follow-up; informed consent of the patient or a legal representative (patients unable to sign the consent form).
Exclusion Criteria
* Children under 18 years old
* No possible follow-up after the first visit
* Refusal to participate in the study
* Patient not registered in the French medical social security national program
18 Years
120 Years
ALL
No
Sponsors
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Clinique Antilles-Guyane
OTHER
Institut National de la Santé Et de la Recherche Médicale, France
OTHER_GOV
University Hospital Center of Martinique
OTHER
Responsible Party
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Principal Investigators
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Patrick Hochedez, MD
Role: PRINCIPAL_INVESTIGATOR
CHU fort de france
Locations
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CHU Pointe-à-Pitre Abymes
Pointe à Pitre, Guadeloupe, France
CHU Martinique
Fort de France, Martinique, France
Countries
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Other Identifiers
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CHU FDF 10/B/13
Identifier Type: -
Identifier Source: org_study_id
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