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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01731353
Other study ID # Fungi001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 2003
Est. completion date December 2026

Study information

Verified date December 2023
Source University of Cologne
Contact Oliver A Cornely, Prof.
Phone +49 221 478
Email oliver.cornely@uk-koeln.de
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this registry is to broaden the knowledge on epidemiology, diagnostic procedures and clinical course of emerging invasive fungal infections.


Description:

The specific objectives are: 1. To determine the fungal species causing invasive fungal infection in different parts of the world. 2. To determine the clinical pattern of disease and document procedures performed for confirmation of the diagnosis. 3. To describe the therapeutic regimens used and their efficacy. 4. To share clinical isolates among the contributors of Fungiscope. 5. To develop molecular biology tools for identification of strains in histopathologically proven invasive fungal infection.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 2026
Est. primary completion date December 2026
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Cultural, histopathological, antigen or DNA evidence of invasive fungal infection Exclusion Criteria: - Infection due to Candida spp., Cryptococcus neoformans, Pneumocystis jiroveci - Endemic fungal infection such as coccidioidomycosis or histoplasmosis - Colonisation or other non-invasive infection

Study Design


Locations

Country Name City State
Germany University Hospital Cologne Cologne NRW

Sponsors (6)

Lead Sponsor Collaborator
University of Cologne Basilea Pharmaceutica, Cidara Therapeutics Inc., F2G Biotech GmbH, Matinas Biopharma, Inc, Pfizer

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Treatment efficacy of emerging fungal infections failure, stable disease, partial response or complete response At 90 days from diagnosis
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