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AspergillusOne-Health: Deciphering Azole Resistance in Aspergillus Fungi Using a One Health Approach

AspergillusOne-Health: Deciphering Azole Resistance in Aspergillus Fungi Using a One Health Approach

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06532227
Acronym
AspergillusOH
Enrollment
1000
Registered
2024-08-01
Start date
2026-09-01
Completion date
2029-08-01
Last updated
2026-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aspergillus Fumigatus Infection

Brief summary

During a two year prospective study onpatients from department's hospitals and centralized by the pneumology department Nantes CH,all respiratory clinical samples will be cultivated for Aspergillus isolation (2900Aspergillusisolates) as standard care. The azole susceptibility pattern of isolates will be determined to itraconazole, voriconazole by subculture on azole- enriched medium at 35°c as primary screen and resistance confirmed by EUCAST Reference metho.In parallel, the relevance of detecting resistance (TR34 and TR46) directly in culture-negative BAL respiratory samples by a qPCR method will be studied in an attempt to reach a greater exhaustiveness of the resistance phenomeno. In case of azole-resistant isolate,patient data such as the underlying disease,date and site of Aspergillus isolation,disease classification,previous azole drug exposure,and home and work geographic allocation,occupation of the patient will be collecte. For all other aspergillus occurrences, underlying disease, previous azole drug exposure,home and work location of the patient will be collected in an attempt to identify risk factor.

Interventions

OTHERNo intervention

No intervention excepted data collection

Sponsors

Nantes University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Patient over 18 years of age * Patient who has given his or her consent to participate in the study * Patient affiliated to a social security scheme * Patient with a respiratory sample taken between 2020 and 2023 for the retrospective cohort and from 2024 for the prospective cohort in which Aspergillus has been isolated * Patients living in the Loire Atlantique and Vendée regions

Exclusion criteria

* Patient under guardianship or legal protection * Patient of no fixed adress

Design outcomes

Primary

MeasureTime frameDescription
Environmental risk factors24 monthsIdentify the "macro" environmental risk factors for acquiring azole-resistant aspergillus.

Secondary

MeasureTime frameDescription
Describe the management and evolution of resistant48 monthsClinical information from each additional patient visit and presence or absence of resistant Aspergillus in home samples.
Risk factors48 monthsIdentify individual risk factors linked to the immediate environment in the patient's home, drug management, between cases and matched controls, etc..

Countries

France

Contacts

CONTACTFrançois-Xavier Blanc, PUPH
xavier.blanc@chu-nantes.fr0240165710

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 25, 2026