Candida PCR Diagnosis Strategy in Patients From Intensive Care Units
Recruiting
N/A
Interventional Study
Candida
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 120 (estimated)
- Sponsor
- University Hospital, Toulouse · Other
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About This Trial
The aim of this study is to evaluate the implementation of a new technique for invasive candidiasis diagnosis by PCR. The main objective will be to evaluate the effect of this strategy on the time required to obtain results in patients from intensive care units with suspected systemic invasive candidiasis. This PCR method could allow an antifungal switch to be made earlier, limiting the appearance…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patient affiliated or benefiting from a social protection system
* Patient (or his/her trusted person) having given free and informed written consent to the investigating physician
* Non-neutropenic patient hospitalised in the Toulouse University Hospital intensive care unit.
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Contacts