New wrist surgery technique under review: will it restore hand function?
NCT ID NCT07667114
First seen Jun 27, 2026 · Last updated Jul 02, 2026 · Updated 1 time
Summary
This study reviews the outcomes of a specific wrist surgery (modified FCR tenodesis) performed on 100 patients with scapholunate ligament tears between 2016 and 2026. The goal is to see how well the wrist works after surgery using a standard questionnaire. The study is observational and looks back at past cases, so it cannot prove the surgery works better than other treatments.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- modified flexor carpi radialis tenodesis (surgical procedure)
- What this could lead to
- If successful, this could confirm that the modified FCR tenodesis is a reliable surgical option for restoring wrist function after scapholunate ligament injury.
- What could go wrong
- This is a retrospective study, not a controlled trial, so results may be influenced by patient selection or missing data. The procedure is surgical and carries typical risks like infection or stiffness.
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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Jul 2026
- Expected to finish
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May 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.
Who is studied
Participation in the study is offered to all eligible patients who underwent a modified flexor carpi radialis (FCR) tenodesis for an SL ligament injury at Waldfriede Hospital between 2016 and 2026.
- Ages
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18 years and older
- 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: * Age: ≥ 18 years * Capable of providing informed consent independently * Availability of written informed consent for the study Exclusion Criteria: * Active malignant disease * Pregnancy at the time of the examination * Presence of SLAC arthritis * Lack of capacity to provide independent consent
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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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Waldfriede Hospital
RECRUITINGBerlin, State of Berlin, 14163, Germany