Actively Recruiting
Prognosis of Disseminated and Cerebral Toxoplasmosis in Intensive Care Evaluating Clinical and Prognostic Differences Using PCR Diagnosis Toxoplasmosis in ICU (TOXIC) Study
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-01-28
200
Participants Needed
1
Research Sites
86 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Toxoplasmosis is a common infection that can become severe enough to require intensive care, especially in people with weakened immune systems. This research aims to evaluate the effects of different anti-infective treatments and to identify clinical and biological differences as well as prognostic factors based on the type of immune suppression. The study focuses on two main forms of the disease: cerebral toxoplasmosis and disseminated toxoplasmosis, with an emphasis on how diagnosis using PCR has changed management. The study observes patients admitted to intensive care with severe toxoplasmosis confirmed by PCR tests from cerebrospinal fluid, blood, bronchoalveolar lavage, or bone marrow. Treatment regimens, including intravenous and oral combinations of drugs like trimethoprim-sulfamethoxazole, pyrimethamine, sulfadiazine, and clindamycin, are monitored, although the study itself does not administer interventions. The research distinguishes between different patient subgroups based on their underlying immunosuppression to better understand treatment impacts and disease progression. Participants are adults hospitalized in intensive care with at least one organ failure and a positive PCR diagnosis within a week before or after ICU admission. Researchers will monitor mortality rates over an 11-year period and collect clinical and biological data to evaluate disease severity and treatment outcomes. The study seeks to improve early detection, identify new at-risk patient categories, and enhance management of severe toxoplasmosis cases in intensive care units.
CONDITIONS
Official Title
Prognosis of Disseminated and Cerebral Toxoplasmosis Hospitalized in Intensive Care in the Era of PCR Diagnosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patient hospitalized in intensive care
- At least 1 organ failure (SOFA score �3 2)
- Positive PCR test for toxoplasmosis from cerebrospinal fluid, blood, bronchoalveolar lavage, or bone marrow within 7 days before or after ICU admission
You will not qualify if you...
- Diagnosis made after death
- Primary outcome data not available
- Patient living and opposed to reuse of their data for this research
AI-Screening
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Trial Site Locations
Total: 1 location
1
Cochin hospital
Paris, France, France, 75014
Actively Recruiting
Research Team
C
Clara Vigneron, MD
R
Romain Sonneville, MD, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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