Actively Recruiting
Prognosis of Disseminated and Cerebral Toxoplasmosis Hospitalized in Intensive Care in the Era of PCR Diagnosis - Toxoplasmosis in ICU (TOXIC)
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-01-28
200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Toxoplasmosis is a common infection that can be severe enough to require intensive care, especially for people with weakened immune systems. This research aims to evaluate how different anti-infective treatments affect patients with severe forms of toxoplasmosis, including cerebral and disseminated types. It also seeks to identify clinical, biological, and prognostic differences based on the type of underlying immunosuppression in these patients. The study observes patients hospitalized in intensive care with confirmed toxoplasmosis diagnosed using polymerase chain reaction (PCR) tests from cerebrospinal fluid, blood, bronchoalveolar lavage, or bone marrow samples. It records the use of various treatment regimens such as oral pyrimethamine-sulfadiazine and intravenous treatments like trimethoprim-sulfamethoxazole or clindamycin combined with pyrimethamine. The study focuses on real-world management without altering treatments and includes patients with at least one organ failure. Participants will be monitored for outcomes including mortality rate in intensive care, hospital mortality, length of stay in intensive care, and duration of mechanical ventilation over an 11-year period. The study collects detailed clinical and biological information to better understand severe toxoplasmosis in immunocompromised patients. Data reuse is subject to patient consent, and the research is observational with no experimental interventions applied.
CONDITIONS
Brief 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 with SOFA score greater than or equal to 2
- Positive PCR test for toxoplasmosis on cerebrospinal fluid, blood, bronchoalveolar lavage, or bone marrow within 7 days before or after ICU admission
You will not qualify if you...
- Post-mortem diagnosis
- Primary outcome data not available
- Patient informed and opposed to reuse of their data in this research
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 11 years
Participants who are hospitalized in intensive care with confirmed toxoplasmosis are observed to collect clinical and biological data related to their condition and treatment.
Ongoing data collection during intensive care stay and hospitalization
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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