Cerebral Toxoplasmosis and AIDS

NCT ID: NCT00803621

Last Updated: 2019-07-05

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

46 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-06-30

Study Completion Date

2013-12-31

Brief Summary

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With a HIV incidence much higher in the DFA than in European French territory, this disease is a major public health problem in these areas, especially in French Guiana.

Cerebral toxoplasmosis is a priority among the opportunistic infections in AIDS patients from the DFA because of its frequency (French West Indies) and of its lethality (French Guiana).

The diagnosis of cerebral toxoplasmosis may be difficult because based only on presumptive clinical and radiological features. The response to specific antitoxoplasmic therapy confirms a posteriori the diagnosis.

In reference to the data collected by the Biological Resource Centre Toxoplasma, in particular in French Guiana, we think that T. gondii strains reactivating in AIDS patients from DFA are genetically different from those reactivating in AIDS patients from Europe, with an increased capacity for dissemination via peripheral blood in the first ones. This more frequent or more prolonged parasitemia could facilitate the diagnosis of cerebral toxoplasmosis by PCR test from peripheral blood samples in AIDS patients from the French departments of America.

Detailed Description

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Conditions

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Cerebral Toxoplasmosis AIDS

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Toxoplasma PCR assay

Toxoplasma PCR assay

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Adult patient (\> 18 years)
* Patient being informed and accepting to participate in the study with signature of informed consent
* HIV positive serology
* Clinical and radiological suspicion of cerebral toxoplasmosis justifying the start of specific antitoxoplasmic therapy

Exclusion Criteria

* Protected patient
* Patient uncovered by social insurance
* Specific antitoxoplasmic therapy already initiated since 72h or more
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Limoges

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Daniel AJZENBERG, PharmD, PhD

Role: STUDY_DIRECTOR

CHU Limoges

Locations

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Service des Maladies Infectieuses - CHU de Pointe à Pitre

Pointe à Pitre, Guadeloupe, France

Site Status

Dermatologie et CISIH- CH Andrée Rosemon

Guyane-Française, Guyane-Française, France

Site Status

Médecine- CH Ouest Guyanais

Guyane-Français, Guyane-Français, France

Site Status

Services Maladies Infectieuses et Tropicales- CHU Fort-de-France

Fort-de-France, , France

Site Status

Maladies Infectieuses et Tropicales - CH Andrée Rosemon

Guyane-Française, , France

Site Status

Countries

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France

References

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Ajzenberg D, Lamaury I, Demar M, Vautrin C, Cabie A, Simon S, Nicolas M, Desbois-Nogard N, Boukhari R, Riahi H, Darde ML, Massip P, Dupon M, Preux PM, Labrunie A, Boncoeur MP. Performance Testing of PCR Assay in Blood Samples for the Diagnosis of Toxoplasmic Encephalitis in AIDS Patients from the French Departments of America and Genetic Diversity of Toxoplasma gondii: A Prospective and Multicentric Study. PLoS Negl Trop Dis. 2016 Jun 29;10(6):e0004790. doi: 10.1371/journal.pntd.0004790. eCollection 2016 Jun.

Reference Type RESULT
PMID: 27355620 (View on PubMed)

Other Identifiers

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I07009

Identifier Type: -

Identifier Source: org_study_id

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