Does nerve healing keep pace with hand recovery after carpal tunnel surgery?

NCT ID NCT07803939

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 04, 2026 · Last updated Sep 04, 2026

Summary

This study follows 100 adults who are already scheduled for carpal tunnel release surgery, a standard procedure to relieve pressure on the median nerve in the wrist. Researchers will measure nerve conduction before surgery and again months later, while also tracking symptoms, hand strength, and daily function through questionnaires and exams. The goal is to see whether improvements in nerve signals match improvements in how the hand actually feels and works. The study does not test any new treatment; it only observes the natural recovery process.

What this could mean

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

Active substance
Carpal tunnel release surgery (standard procedure)
What this could lead to
If it works, this could help doctors predict which patients will recover hand function fastest after carpal tunnel surgery and tailor follow-up care.
What could go wrong
This is an observational study, so it cannot prove cause and effect. Results may not apply to all patients, and nerve tests may not fully capture how a person feels or functions.

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

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Nov 2026

An estimate. End dates often move.

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 75 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: * Age between 18 and 75 years. * Clinical and electrophysiological diagnosis of carpal tunnel syndrome. * Scheduled to undergo primary carpal tunnel release surgery based on routine clinical evaluation. * Availability of a preoperative nerve conduction study. * Ability to understand and complete the study assessments and questionnaires. * Ability to read and understand Turkish. * Willingness to participate and provide written informed consent. * Ability and willingness to attend the planned postoperative follow-up assessments. For participants with bilateral carpal tunnel syndrome who undergo unilateral surgery during the study period, only the operated hand will be included in the study. Two hands from the same participant will not be analyzed as independent observations. Exclusion Criteria: * Previous carpal tunnel release surgery on the study hand. * Planned revision carpal tunnel surgery. * Electrophysiological evidence of generalized polyneuropathy. * Another peripheral neuropathy affecting the median nerve or function of the study hand. * Active cervical radiculopathy or brachial plexopathy. * A central or peripheral neurological disorder that substantially affects upper-extremity function. * History of major trauma or surgery involving the study hand or wrist that may affect outcome assessments. * Active inflammatory rheumatologic disease. * Pregnancy. * Uncontrolled systemic disease that may interfere with surgery, assessment, or follow-up. * Cognitive or communication impairment that prevents completion of the study assessments. * Inability to complete the planned postoperative follow-up assessments. Participants with controlled diabetes mellitus will not be excluded solely because of diabetes. However, participants with electrophysiologically confirmed generalized polyneuropathy will be excluded. Diabetes status will be recorded and considered as a potential confounding variable in the analyses.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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