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

N

Nantes University Hospital (NUH)

Status

Not yet enrolling

Conditions

Aspergillus Fumigatus Infection

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT06532227
RC23_0008

Details and patient eligibility

About

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.

Enrollment

1,000 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

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

Trial design

1,000 participants in 2 patient groups

Group control : patient without resistance
Description:
control patients with susceptible Aspergillus.
Treatment:
Other: No intervention
Group resistant : patient without resistance
Description:
Cases are patients with resistant Aspergillus
Treatment:
Other: No intervention

Trial contacts and locations

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Central trial contact

François-Xavier Blanc, PUPH

Data sourced from clinicaltrials.gov

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