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TerminatedNCT02863588TREXOUpdated Sep 8, 2021

Determination of Genetic Susceptibility in Severe Recurrences of Ocular Toxoplasmosis

An interventional study of seropositive for Toxoplasma gondii in Toxoplasmosis Infection, Genotype II and Ocular Toxoplasmosis With Recurrences, sponsored by University Hospital, Strasbourg, France. Terminated at 1 site in France. Open to participants aged 12 Years and older. Per ClinicalTrials.gov, last updated 2021-09-08.

Sponsored by University Hospital, Strasbourg, France · Not applicable, Interventional, and Basic science

Why this study was terminated
recruitment difficulty
Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Not applicable
Ages
12 Years and older
Sex
All
01

Study 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.

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Conditions studied

  • Toxoplasmosis Infection
  • Genotype II
  • Ocular Toxoplasmosis With Recurrences
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In context

Toxoplasmosis

36 studies on the registry are indexed under Toxoplasmosis; 9 are open to participants now.

This study's enrollment of 16 is below the median of 105 across 20 interventional studies indexed under Toxoplasmosis.

Browse Toxoplasmosis studies →

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 968 studies on the registry; 344 are open to participants now.

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

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Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

Exclusion Criteria:

  • Parents seronegative for T. gondii infection
  • Infection with others genotypes than type II
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
16 participants (actual)

Study arms

  • Experimental
    seropositive for Toxoplasma gondii

    Biological: seropositive for Toxoplasma gondii

Interventions

  • Biologicalseropositive for Toxoplasma gondii

    blood sample

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What researchers measure

Primary outcomes

  1. 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

    Time frame: This analysis will be performed on a blood sample taken in patients included in the inclusion visit

07

Study locations

1 site
  • University Hospital, Strasbourg, france
    Strasbourg, 67000, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 8, 2021, 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
NCT02863588
Lead sponsor
University Hospital, Strasbourg, France
Responsible party
Sponsor
First posted
Aug 11, 2016
Start date
Mar 30, 2017
Primary completion
Nov 11, 2019
Completion
Nov 11, 2019
Last update
Sep 8, 2021

Study contacts

Arnaud SAUER, MD
principal investigator · University Hospital, Strasbourg, France

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 terminated, as verified in Aug 2021. You cannot join it, but the record below documents what was studied.

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