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Ultra-High field MRI could sharpen diagnosis of foot injuries
NCT ID NCT04441983
First seen Jul 10, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This study explores whether a 7 Tesla MRI scanner can produce clearer images of the foot and ankle than standard MRI. Researchers will scan people with known foot problems—like plantar plate tears or Morton neuroma—and healthy volunteers to see if the higher-powered machine detects these issues more accurately. The goal is to improve diagnosis of complex foot anatomy and injuries.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 7 Tesla MRI
- What this could lead to
- If successful, this could make 7 Tesla MRI a more accurate tool for diagnosing foot and ankle injuries, potentially improving treatment decisions.
- What could go wrong
- This is an early imaging study, not a treatment trial. The new MRI may not prove more useful than current scans, and its availability is limited.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2021
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- 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.
Who is studied
Patients who have undergone a forefoot MRI for clinical indications (or previous study) will be enrolled
- 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: * Informed consent as documented by signature (Appendix Informed Consent Form) * at least 18 years old * Study group: Patients with specific pathologies (i.e. Morton neuroma, tendon tears, plantar plate tears) as proven by 1,5 or 3T MRI or asymptomatic subjects (to look at the normal microanatomy of different structures, mainly the plantar plate) * Control group: No evidence of the respective pathology. Exclusion Criteria: * previous foot/ extremities surgery with metal in vivo * pregnancy or breast feeding * any MRI contra-indications
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Balgrist University Hospital
RECRUITINGZurich, Canton of Zurich, 8008, Switzerland
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