Can MRI replace CT scans for lung fibrosis in scleroderma?
NCT ID NCT03207997
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a special MRI technique can measure lung stiffness in people with scleroderma, a disease that often causes lung scarring. Researchers enrolled 24 adults and compared MRI results to standard lung function tests. The goal was to see if MRI could offer a safer, radiation-free way to track lung damage.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a safer, radiation-free way to monitor lung scarring in scleroderma patients.
- What could go wrong
- This is a small feasibility study with only 24 participants, so results may not apply broadly. The MRI technique is still experimental and not yet ready for routine use.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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24 people
The number who actually took part.
- Started
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Sep 2017
- Finished
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Mar 2018
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients aged 18 years or older * Having a diagnosis of diffuse or limited cutaneous systemic sclerosis (EULAR criteria 2013) * Referred for cardiac MRI * Having a thoracic assessment (CT and PFT) within 3 months * with social security insurance * Having given their consent Exclusion Criteria: * MRI-related contraindications: * Pacemaker * Mechanical heart valve * Intracranial vascular clips before 1993 * Foreign metallic ocular body * Cochlear Implant * Claustrophobic patients * Pregnant woman * Disease in exacerbation * Orthopnea * Inability to hold a 17-second apnea * Patients in the exclusion period following a previous search * Absence of thoracic evaluation by CT and PFT within 3 months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cochin Hospital
Paris, Paris, 75014, France
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Other studies related to the condition(s) this trial covers.
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