Hand splint may boost recovery after tendon surgery
NCT ID NCT07290348
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a custom dynamic hand splint helps improve hand movement after surgery to repair torn extensor tendons. Forty adults aged 20-40 with tendon injuries in zones 5 or 6 participated. After three weeks of wearing a static splint, one group used the dynamic splint during the day for two months, while the other group did not. Researchers measured wrist and finger joint range of motion before treatment, after one month, and at the end.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- customized dynamic hand splint
- What this could lead to
- If effective, this splint could help people regain better hand movement after tendon repair surgery, improving daily function.
- What could go wrong
- This is a small, completed study with only 40 participants. Results may not apply to everyone, and the splint might not provide significant benefit over standard care.
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.
- Phase
-
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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40 people
The number who actually took part.
- Started
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Aug 2023
- Finished
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Jan 2025
- 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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20 to 40 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 are both males and females. * Their age will be in the range of 20-40 years. * All patients suffering from extensor tendon injuries in zone 5 or 6. * All patients undergo extensor tendon repair surgery. * All patients will begin the treatment program from the third week post-operative. * All patients enrolled in the study will have their informed consent. Exclusion Criteria: * The potential participants will be excluded if they meet one of the following criteria: * Patients with associated diseases (diabetes mellitus, infectious diseases, autoimmune disease) that will interfere with the healing process. * Patients taking medication that alters the healing process (e.g., corticosteroids, chemotherapy, or radiation). * Pregnancy or epilepsy. * Elderly patients. * Skin disease.
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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
-
Mansoura international hospital, Dakahlia government, Egypt
Al Mansurah, Egypt
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