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NCT04874441: CANDI-PCR

Candida PCR Diagnosis Strategy in Patients From Intensive Care Units

Recruiting now NA Last updated 2 August 2024
What this trial tests

NA trial testing Diagnosis strategy based on C. glabrata / krusei PCR in Candida in 120 participants. Currently enrolling.

Timeline
19 May 2022
Primary endpoint
1 August 2025
1 August 2025

Quick facts

Lead sponsorUniversity Hospital, Toulouse
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment120
Start date19 May 2022
Primary completion1 August 2025
Estimated completion1 August 2025
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Toulouse

Who can join

18 and older, any sex, with Candida. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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 of resistance and reducing the cost of antifungals for healthcare facilities.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Candida

Currently open trials in the same condition.

Other University Hospital, Toulouse trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04874441.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing