Actively Recruiting

Age: 18Years - 100Years
All Genders
ID06305468

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

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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

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

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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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