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Hand splint may boost recovery after tendon surgery

NCT ID NCT07290348

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

40 people

The number who actually took part.

Started

Aug 2023

Finished

Jan 2025

Lead sponsor

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

20 to 40 years

Sex

Anyone

Healthy volunteers

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

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.

extensor tendons of finger anomalies Hapnes Boman Skeie syndrome

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

More trials for these conditions

Other studies related to the condition(s) this trial covers.