Skip to content

Diagnostic Strategy for Pulmonary Aspergillosis: A Prospective Observational Study

Diagnostic Strategy for Pulmonary Aspergillosis: A Prospective Observational Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128541
Enrollment
Unknown
Registered
2026-07-22
Start date
2026-07-25
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Pulmonary Aspergillosis

Interventions

Gold Standard:Proven Case: Identification of Aspergillus hyphae via microscopy or culture from needle aspiration or biopsy specimens obtained from a sterile site, accompanied by tissue damage
or culture of Aspergillus from sterile samples collected from the lesion site
or detection of Aspergillus DNA in formalin-fixed, paraffin-embedded tissues through PCR amplification and sequencing. Clinically Diagnosed Case: Must meet at least one criterion from each of the foll
Index test:Galactomannan (GM) Antigen PCR Culture

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years; 2.Strong clinical suspicion of pulmonary aspergillosis based on a comprehensive assessment of symptoms, signs, and imaging by a clinician; 3.Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating women; 2.Individuals unable to cooperate with the study or provide informed consent; 3.Cases where clinical data are expected to be insufficient for final diagnostic grouping.

Design outcomes

Primary

MeasureTime frame
Galactomannan (GM) Antigen;Aspergillus-specific IgG;Aspergillus Polymerase Chain Reaction;(1,3)-ß-D-Glucan Detection Assay;Chest CT;Microbial Culture;

Countries

China

Contacts

Public ContactXiang Tong

West China Hospital of Sichuan University

tongxiang@scu.edu.cn+86 187 0285 3986

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026