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Invasive Candidiasis in Critical Care

Status: Recruiting
Intervention Type: Diagnostic test, Other
Study Type: Observational
SUMMARY

The combination of acute phase marker monitoring and the T2Candida assay (name of the test) will represent an acceleration of the identification of the causative agent of mycotic infection, a significant improvement in the specificity and positive predictive value of this strategy in the diagnosis of invasive candidiasis and candidemia in ICU patients, thereby improving the clinical condition of patients and reducing the cost of specific antifungal therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Healthy Volunteers: f
View:

• critically ill patients

• new onset sepsis

• rise in body temperature \>38°C according to The Third Consensus Definitions for Sepsis and Septic Shock

• colonization with Candida spp. from more than 1 non-sterile site

• body temperature \>38 °C despite 5 days of broad-spectrum antibiotic therapy with the presence of at least 1 of the following risk factors: abdominal surgery, secondary peritonitis, pancreatitis, central venous catheter (CVC) insertion, total parenteral nutrition (CPV), dialysis, steroid therapy, immunosuppressive therapy, or liver transplantation

• microbiological test results will be reviewed and categorized based on whether Candida sp. is isolated from at least 2 non-sterile sites (±3 days) and whether there is an alternative microbiological diagnosis.

Contact Information
Primary
Jiří Hynčica
jiri.hyncica@fno.cz
0042059737
Time Frame
Start Date: 2024-04-11
Estimated Completion Date: 2027-12
Participants
Target number of participants: 100
Treatments
Patients with suspected invasive candidiasis
Patients with suspected invasive candidiasis will be enrolled in this study arm.
Related Therapeutic Areas
Sponsors
Leads: University Hospital Ostrava
Collaborators: University Hospital, Motol

This content was sourced from clinicaltrials.gov