Double scan strategy aims to catch wrist tears that single MRI misses
NCT ID NCT07826208
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Wrist injuries involving small ligaments and cartilage can be hard to see on standard imaging. This study tests whether adding CT arthrography to MR arthrography helps doctors detect more internal wrist damage than MR arthrography alone. Participants aged 15 to 60 with suspected wrist ligament, cartilage, tendon, or hidden bone injuries receive an ultrasound-guided contrast injection into the wrist joint, followed by a high-resolution CT scan and an MR arthrography scan. Researchers compare the two imaging methods to see how often the combined approach finds lesions that MR arthrography missed or left unclear.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- combined CT arthrography and MR arthrography, two imaging scans done after a contrast dye is injected into the wrist joint
- What this could lead to
- If the combined scans detect more wrist injuries than MR arthrography alone, doctors could gain a clearer picture of hidden ligament tears and cartilage damage, which may guide treatment decisions.
- What could go wrong
- This is a small, single-center study with 60 planned participants, so its findings may not apply to every clinic or scanner. The extra CT scan adds radiation exposure and requires a joint injection, and some wrist injuries may still go undetected.
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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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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2027
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.
- Ages
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15 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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 15 to 60 years. * Clinically suspected ligamentous, cartilage, tendon, or occult osseous wrist injury. * Patients scheduled for MR arthrography of the wrist. Exclusion Criteria: * History of previous wrist surgery. * Acute fractures requiring emergency management. * Active wrist infection. * Contraindications to iodinated or gadolinium-based contrast agents. * Regional metallic implants causing significant imaging artifacts. * Pregnancy.
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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