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Comparison Between Ultra-low-dose Computed Tomography and Lung MRI in Cystic Fibrosis (UBD-IRM)

Primary Purpose

Cystic Fibrosis

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
CT scanner
Lung MRI
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Cystic Fibrosis focused on measuring Magnetic resonance imaging, Multidetector computed tomography

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 year-old
  • Diagnosis of cystic fibrosis provided by genetic and swear test
  • Chest CT acquisition performed as part of the standard follow-up
  • Patient with social security or health insurance
  • Informed consent

Exclusion Criteria:

  • MRI contraindication
  • Orthopnea
  • Inability to hold breath for 17 seconds
  • No spirometry planned the same day
  • Lung transplant patient

Sites / Locations

  • Cochin hospitalRecruiting

Outcomes

Primary Outcome Measures

Reproducibility of visual score between imaging modalities
Reproducibility disease severity measured by the Helbich scoring system with conventional CT as gold standard

Secondary Outcome Measures

Intra and interobserver reproducibility of visual scores
Intra and interobserver reproducibility of the Helbich score for each imaging modality
Correlation between visual scores and pulmonary function
Correlation between the Helbich score for each imaging modality and forced expiratory volume in 1 second (FEV1)
Correlation between air trapping at MRI and pulmonary function test
Correlation between air trapping, measured by comparing inspiratory to expiratory MRI images, and forced expiratory volume at one second (FEV1)

Full Information

First Posted
October 5, 2020
Last Updated
September 4, 2023
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT04644471
Brief Title
Comparison Between Ultra-low-dose Computed Tomography and Lung MRI in Cystic Fibrosis
Acronym
UBD-IRM
Official Title
Comparison Between Ultra-low-dose Computed Tomography and Lung MRI for Morphological Assessment of Lung Disease in Adult Cystic Fibrosis Patients
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 5, 2021 (Actual)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
August 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the performances of ultra-low dose computed tomography (CT) and lung magnetic resonance imaging (MRI) for morphological assessment of cystic fibrosis-related lung disease and to compare their performances to conventional low dose CT
Detailed Description
Cystic fibrosis (CF) is a recessive autosomal disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene that encodes for an epithelial chloride channel involved in ion and fluid transport. CF is the most common inherited disease in Caucasians and disease severity mainly depends on the degree of lung involvement, which can lead to terminal respiratory failure Disease monitoring of CF-related lung disease rely on functional assessment and complimentary morphological assessment. Conventional low-dose chest computed tomography (CT) is currently the gold standard for the morphological assessment of CF-related lung disease but ultra-low dose chest CT and high-resolution magnetic resonance imaging (MRI) of the lung using UTE sequences have been recently developed and allow important radiation reduction of radiation dose exposure. However the performances of these 2 competing imaging methods remains to be compared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
Keywords
Magnetic resonance imaging, Multidetector computed tomography

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Diagnostic Test
Intervention Name(s)
CT scanner
Intervention Description
1 conventional low dose inspiratory acquisition and 1 ultra-low-dose inspiratory acquisition
Intervention Type
Diagnostic Test
Intervention Name(s)
Lung MRI
Intervention Description
3 UTE sequences (free breathing, inspiratory and expiratory) and 1 T2 sequence
Primary Outcome Measure Information:
Title
Reproducibility of visual score between imaging modalities
Description
Reproducibility disease severity measured by the Helbich scoring system with conventional CT as gold standard
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Intra and interobserver reproducibility of visual scores
Description
Intra and interobserver reproducibility of the Helbich score for each imaging modality
Time Frame
1 day
Title
Correlation between visual scores and pulmonary function
Description
Correlation between the Helbich score for each imaging modality and forced expiratory volume in 1 second (FEV1)
Time Frame
1 day
Title
Correlation between air trapping at MRI and pulmonary function test
Description
Correlation between air trapping, measured by comparing inspiratory to expiratory MRI images, and forced expiratory volume at one second (FEV1)
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 year-old Diagnosis of cystic fibrosis provided by genetic and swear test Chest CT acquisition performed as part of the standard follow-up Patient with social security or health insurance Informed consent Exclusion Criteria: MRI contraindication Orthopnea Inability to hold breath for 17 seconds No spirometry planned the same day Lung transplant patient
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Guillaume CHASSAGNON, PhD
Phone
+33 1 58 41 53 66
Email
guillaume.chassagnon@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Adèle BELLINO
Phone
+33 158411195
Email
adele.bellino@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie-Pierre REVEL, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Study Director
Facility Information:
Facility Name
Cochin hospital
City
Paris
ZIP/Postal Code
75014
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guillaume CHASSAGNON, PhD
Phone
+33 1 58 41 53 66
Email
guillaume.chassagnon@aphp.fr
First Name & Middle Initial & Last Name & Degree
Adèle BELLINO
Phone
+ 33 158411195
Email
adele.bellino@aphp.fr

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25768672
Citation
Dournes G, Grodzki D, Macey J, Girodet PO, Fayon M, Chateil JF, Montaudon M, Berger P, Laurent F. Quiet Submillimeter MR Imaging of the Lung Is Feasible with a PETRA Sequence at 1.5 T. Radiology. 2015 Jul;276(1):258-65. doi: 10.1148/radiol.15141655. Epub 2015 Mar 13. Erratum In: Radiology. 2016 Apr;279(1):328.
Results Reference
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PubMed Identifier
26843010
Citation
Dournes G, Menut F, Macey J, Fayon M, Chateil JF, Salel M, Corneloup O, Montaudon M, Berger P, Laurent F. Lung morphology assessment of cystic fibrosis using MRI with ultra-short echo time at submillimeter spatial resolution. Eur Radiol. 2016 Nov;26(11):3811-3820. doi: 10.1007/s00330-016-4218-5. Epub 2016 Feb 2.
Results Reference
background
PubMed Identifier
31051201
Citation
Chassagnon G, Martin C, Ben Hassen W, Freche G, Bennani S, Morel B, Revel MP. High-resolution lung MRI with Ultrashort-TE: 1.5 or 3 Tesla? Magn Reson Imaging. 2019 Sep;61:97-103. doi: 10.1016/j.mri.2019.04.015. Epub 2019 Apr 30.
Results Reference
background
PubMed Identifier
30835186
Citation
Chassagnon G, Martin C, Marini R, Vakalopolou M, Regent A, Mouthon L, Paragios N, Revel MP. Use of Elastic Registration in Pulmonary MRI for the Assessment of Pulmonary Fibrosis in Patients with Systemic Sclerosis. Radiology. 2019 May;291(2):487-492. doi: 10.1148/radiol.2019182099. Epub 2019 Mar 5.
Results Reference
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Comparison Between Ultra-low-dose Computed Tomography and Lung MRI in Cystic Fibrosis

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