Actively Recruiting

All Genders
ID03450005

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

All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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)

Surveillance

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

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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

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