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Hand surgery showdown: which stitch count wins?

NCT ID NCT07626190

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compared two surgical techniques for repairing injured flexor tendons in the hand (Zone II). One technique uses four strands of suture, the other uses six. The goal was to see which method leads to better hand function and fewer problems like tendon rupture or scarring. The study involved 136 adults aged 18 to 50 with recent hand tendon injuries.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
surgical repair technique (four-strand or six-strand core suture)
What this could lead to
If one technique proves better, it could become the preferred method for repairing hand tendon injuries, leading to improved hand function and fewer complications.
What could go wrong
This is a completed study with 136 participants, so results are available but may not apply to all patients. The study is not blinded, which could introduce bias.

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

136 people

The number who actually took part.

Started

Jan 2026

Finished

Apr 2026

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

18 to 50 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: * Male or female participants. * Age 18 to 50 years. * Zone II flexor tendon injury of the hand. * Presentation within one week of injury. * Willingness to participate and provide informed consent. * Ability to comply with the postoperative rehabilitation protocol. Exclusion Criteria: * Injuries that interfere with postoperative rehabilitation. * Extensive soft tissue damage associated with the tendon injury. * Previous tendon injury in the same digit or hand region. * Previous surgery in the same affected area. * Non-compliance or anticipated inability to comply with the postoperative rehabilitation protocol. * Evidence of a psychological or personality disorder that may affect participation or outcome assessment. * Systemic illness that may compromise wound or tendon healing (e.g., uncontrolled diabetes mellitus, connective tissue disorders, severe vascular disease).

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Allied Hospital, Faisalabad Medical University

    Faisalabad, Punjab Province, 00000, Pakistan

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