Invasive Fungal Disease Clinical Trial
— FungiScopeOfficial title:
FungiScope - A Global Emerging Fungal Infection Registry
| 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 |
The objective of this registry is to broaden the knowledge on epidemiology, diagnostic procedures and clinical course of emerging invasive fungal infections.
| 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 |
| Country | Name | City | State |
|---|---|---|---|
| Germany | University Hospital Cologne | Cologne | NRW |
| Lead Sponsor | Collaborator |
|---|---|
| University of Cologne | Basilea Pharmaceutica, Cidara Therapeutics Inc., F2G Biotech GmbH, Matinas Biopharma, Inc, Pfizer |
Germany,
| 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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