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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02863588
Other study ID # 6433
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date March 30, 2017
Est. completion date November 11, 2019

Study information

Verified date August 2021
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Ocular toxoplasmosis (OT) is a major cause of visual impairment worldwide. OT is responsible for 30 to 50% of posterior uveitis. It is characterized by dormant infections that may reactivate without known reasons, causing severe irreversible visual loss. The overall recurrence rate of OT in Europe is greater than 80% for patients and may range from one episode to 11 episodes (1% of OT) in the most extreme cases. Current treatments do not reduce the risk of recurrences and the risk of toxoplasmosis recurrence cannot be predicted in these immunocompetent patients. These clinical and biological expression changes might be related to an individual genetic susceptibility of each patient. The advanced analysis of the entire genome now possible to consider the project.


Recruitment information / eligibility

Status Terminated
Enrollment 16
Est. completion date November 11, 2019
Est. primary completion date November 11, 2019
Accepts healthy volunteers No
Gender All
Age group 12 Years and older
Eligibility Inclusion Criteria: - seropositive for Toxoplasma gondii (for patient and parents) - Infection with genotype II (for patient and parents) - ocular toxoplasmosis recurrences >5 (patients only) Exclusion Criteria: - Parents seronegative for T. gondii infection - Infection with others genotypes than type II

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
seropositive for Toxoplasma gondii
blood sample

Locations

Country Name City State
France University Hospital, Strasbourg, france Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Highlighting of genetic mutations associated with the susceptibility to Toxoplasma gondii.severe eye recurrences. Mutation analysis will be done by exome sequencing of the subjects included in this study This analysis will be performed on a blood sample taken in patients included in the inclusion visit