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PCR for Aspergillus Fumigatus in Blood and Bronchoalveolar Lavage Fluid for Monitoring Cases of Invasive Aspergillosis: What is Its Prognostic Value

PCR for Aspergillus Fumigatus in Blood and Bronchoalveolar Lavage Fluid for Monitoring Cases of Invasive Aspergillosis: What is Its Prognostic Value

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07313527
Acronym
ASP
Enrollment
100
Registered
2026-01-02
Start date
2025-03-17
Completion date
2026-02-28
Last updated
2026-01-02

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

Conditions

Invasive Pulmonary Aspergillosis

Keywords

Invasive Pulmonary Aspergillosis, Aspergillus fumigatus PCR, Bronchoalveolar lavage fluid

Brief summary

Aspergillus fumigatus PCR is currently used in conjunction with serum galactomannan to support the diagnosis of invasive aspergillosis or for monitoring at-risk patients not receiving antifungal prophylaxis. A positive result and a high titer are thought to be associated with the advanced stage of the disease and the fungal load. However, there is limited data on this subject, and no study has primarily focused on the variation of PCR levels during treatment and its potential correlation with treatment efficacy.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients aged 18 years or older * Positive Aspergillus fumigatus PCR on serum or bronchoalveolar lavage fluid at diagnosis, performed at the Strasbourg University Hospital between January 1, 2017, and December 31, 2024.

Exclusion criteria

* No subsequent Aspergillus fumigatus PCR (\>24h) * No diagnosis of probable or proven invasive aspergillosis (EORTC/MSGERC 2020 criteria) * Effective antifungal treatment against Aspergillus initiated before the first PCR * Death \<72h after starting antifungal treatment

Design outcomes

Primary

MeasureTime frameDescription
Death rate at day 30 in patients with a positive follow-up PCR (blood or bronchoalveolar lavage)Day 30 post-antifungal treatmentDeath rate at day 30 in patients with a positive follow-up PCR (blood or bronchoalveolar lavage) after the start of treatment

Countries

France

Contacts

Primary Contactbaptiste Hoellinger, MD
baptiste.hoellinger@chru-strasbourg.fr33 3 69 55 05 45

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026