Study of a Cohort of Non-HIV Immunocompromised Patients With Toxoplasmosis at the Strasbourg University Hospital
TOXO
Retrospective Descriptive Study of a Cohort of Non-HIV Immunocompromised Patients With Toxoplasmosis at the Strasbourg University Hospital From 2010 to 2023
1 other identifier
observational
30
1 country
1
Brief Summary
Toxoplasmosis in HIV-positive individuals is well-studied and has a codified management protocol, which is not the case for other immunodeficiencies, except for recent recommendations in the context of hematopoietic stem cell transplantation. A description of this population is necessary to estimate the number of patients affected and to define their specific management (diagnosis, treatment, prevention).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Feb 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 2, 2025
CompletedFirst Submitted
Initial submission to the registry
December 9, 2025
CompletedFirst Posted
Study publicly available on registry
December 23, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 25, 2026
CompletedDecember 23, 2025
December 1, 2025
12 months
December 9, 2025
December 9, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Overall patient survival rates
Up to 1 year
Eligibility Criteria
Adult subject (≥18 years) with a positive toxoplasmosis PCR test (regardless of tissue)
You may qualify if:
- Adult (≥18 years)
- Immunocompromised (i.e., solid organ transplant recipient, hematological malignancy, cancer patient, patient treated with immunosuppressive therapy or therapy affecting the immune system by any mechanism, hematopoietic stem cell transplant recipient, patient with an autoimmune disease or immunodeficiency, whether primary or secondary).
- At least one positive toxoplasmosis PCR test (regardless of tissue)
You may not qualify if:
- Subject who has expressed opposition to the reuse of their data for scientific research.
- HIV positive
- Congenital toxoplasmosis
- Isolated ocular toxoplasmosis in immunocompetent individuals
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Service d'immunologie clinique - Hôpitaux Universitaires de Strasbourg
Strasbourg, 67091, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 9, 2025
First Posted
December 23, 2025
Study Start
February 2, 2025
Primary Completion
February 1, 2026
Study Completion
February 25, 2026
Last Updated
December 23, 2025
Record last verified: 2025-12