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CompletedNCT03265366ABPA-MRUpdated May 14, 2026

Diagnostic Value of MRI for Allergic Broncho-Pulmonary Aspergilloses

An interventional study of MRI and CT scan (standard reference) in Allergic Bronchopulmonary Aspergilloses, sponsored by University Hospital, Bordeaux. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-14.

Sponsored by University Hospital, Bordeaux · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

The aim of the study is to compare the concordance between chest computerized tomography-scan (CTscan) and Magnetic resonance Imaging (MRI) for the description of the abnormalities seen in Allergic BronchoPulmonary Aspergillosis (ABPA).

Read the detailed description

The ABPA is responsible for pulmonary exacerbations in chronic bronchial diseases. The treatment of ABPA consists in systemic corticosteroids and anti fungal therapy, which can have severe side effects. The diagnosis is difficult, based on several but non-specific characteristics. One of the radiologic abnormalities on CTscan could be more specific : high attenuation in impacted mucus, but this sign is found in about 30% of cases. Recent articles and investigators experience seem to demonstrate that MRI could provide an interesting tool for ABPA diagnosis, studying the signal of bronchial impactions. The aim of the study is to describe the MRI characteristics of patients with ABPA and compare the results with those obtained by CTscan, and in order to determine if there is a specific signal of impaction in ABPA.

02

Conditions studied

  • Allergic Bronchopulmonary Aspergilloses

Keywords

  • Ultrashort echo time magnetic resonance imaging
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • study patients have a diagnosis of ABPA
  • control patients have severe asthma
  • All the patients are ≥ 18 years old, have social security care, signature of consent form

Exclusion criteria

Exclusion Criteria:

  • cystic fibrosis
  • other type of aspergilloses
  • contraindication for MRI
  • woman without effective contraception
04

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
25 participants (actual)

Study arms

  • Experimental
    ABPA

    15 patients with ABPA

    Device: MRI · Device: CT scan (standard reference)

  • Active comparator
    Severe asthma

    12 patients with severe asthma

    Device: MRI · Device: CT scan (standard reference)

Interventions

  • DeviceMRI

    It will be performed on a 1.5-Tesla MR scanner (MAGNETOM Avanto, Siemens Healthcare, Erlangen, Germany), without injection or inhalation of contrast agent.

  • DeviceCT scan (standard reference)

    It will be performed on a 16 (Sensation 16, Siemens®) or 64 channels (Definition 64, Siemens®), without contrast agent injection.

05

What researchers measure

Primary outcomes

  1. Concordance between chest CT scan and MRI for bronchial and pulmonary signs of ABPA (bronchiectases, infiltrates, impactions)

    Measured by a kappa test

    Time frame: Day 0

06

Study locations

1 site
  • CHU de Bordeaux
    Pessac, 33604, France
07

References and documents

Publications

  • Dournes G, Berger P, Refait J, Macey J, Bui S, Delhaes L, Montaudon M, Corneloup O, Chateil JF, Marthan R, Fayon M, Laurent F. Allergic Bronchopulmonary Aspergillosis in Cystic Fibrosis: MR Imaging of Airway Mucus Contrasts as a Tool for Diagnosis. Radiology. 2017 Oct;285(1):261-269. doi: 10.1148/radiol.2017162350. Epub 2017 May 22. PubMed 28530849 ↗
08

Registry details

Key details

Study ID
NCT03265366
Lead sponsor
University Hospital, Bordeaux
Responsible party
Sponsor
First posted
Aug 29, 2017
Start date
Sep 14, 2017
Primary completion
Jan 24, 2020
Completion
Jan 24, 2020
Last update
May 14, 2026

Study contacts

Julie MACEY, MD
principal investigator · University Hospital, Bordeaux

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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