Actively Recruiting
ECMM Candida Registry - CandiReg: Observational Study on Invasive Candida Infections and Antifungal Resistance
Led by University of Cologne · Updated on 2023-12-12
2000
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are conducting the European Confederation of Medical Mycology (ECMM) Candida Registry, called CandiReg, to improve understanding of invasive Candida infections. The study aims to gather comprehensive data on the global occurrence, clinical progression, molecular features, and antifungal resistance of invasive Candida infections. It also seeks to identify patient risk groups, assess mortality and costs related to these infections, and support future research and outbreak responses. The study uses a web-based registry to collect information on invasive Candida infections worldwide. It documents diagnostic methods, treatment approaches including first-line and salvage therapies, adherence to guidelines, and their effects on patient survival. The registry also collects Candida isolates for molecular analysis and resistance gene evaluation to track trends over time and support guideline development. Participants diagnosed with invasive Candida infections contribute clinical data and isolates, while matched controls from the same hospitals are included for comparison. Researchers monitor incidence, mortality, molecular characteristics, susceptibility testing, and resistance development up to 100 weeks after diagnosis. Treatment efficacy and the clinical course of disease are also assessed. The study provides long-term observation without administering experimental treatments, with participation lasting as long as data collection continues.
CONDITIONS
Brief Title
ECMM Candida Registry - CandiReg
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Cultural, histopathological, antigen or DNA evidence of invasive Candida infection
- Hepatosplenic candidiasis with signs of disseminated Candida infection without culture, histological or microscopic evidence
- Case controls matched by demographics, underlying diseases, risk factors, and hospitalization duration at the same hospital
You will not qualify if you...
- Colonization or other non-invasive Candida infections such as superficial skin infections
- Candiduria without dissemination
- Presence of Candida species in stool without invasive infection
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 100 weeks
Participants are observed to describe the incidence, clinical patterns, and treatment outcomes of invasive Candida infections.
Visits as needed for clinical assessments and data collection
Trial Site Locations
Total: 1 location
1
University Hospital Cologne
Cologne, North Rhine-Westphalia, Germany, 50937
Actively Recruiting
Research Team
O
Oliver Cornely, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here