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Ultrasound may reveal hidden clues in carpal tunnel syndrome

NCT ID NCT07752797

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 07, 2026 · Last updated Sep 17, 2026 · Updated 2 times

Summary

This study looks at how the severity of carpal tunnel syndrome relates to ultrasound images of the nerve, nerve conduction tests, hand grip strength, and pain sensitivity. Researchers will assess 90 adults with the condition using these measures during a single visit. The goal is to better understand the links between structural, electrical, and functional changes, which could improve clinical evaluation and patient care.

What this could mean

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

What this could lead to
If successful, this study could improve how doctors assess carpal tunnel syndrome, potentially leading to better diagnosis and treatment planning.
What could go wrong
This is an observational study, so it cannot prove cause and effect. The findings may not apply to all patients, and the study does not test any treatment.

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

109 people

The number who actually took part.

Started

Jun 2026

Finished

Jul 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.

Who is studied

The study population will consist of adult patients (≥18 years) with clinically suspected and electrophysiologically confirmed carpal tunnel syndrome who are evaluated in the Physical Medicine and Rehabilitation outpatient clinic. Participants will be classified into mild, moderate, and severe groups according to electrophysiological severity.

Ages

18 to 65 years

Sex

Anyone

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: * Adults aged 18 years or older * Clinical findings consistent with carpal tunnel syndrome * Carpal tunnel syndrome confirmed by electroneuromyography * Ability to understand and complete the study assessments * Provision of written informed consent Exclusion Criteria: * Previous carpal tunnel release surgery * History of fracture, major trauma, or surgery involving the assessed wrist or hand * Cervical radiculopathy, brachial plexopathy, or other peripheral neuropathy affecting the upper extremity * Polyneuropathy * Inflammatory rheumatic disease or active infection involving the assessed upper extremity * Severe neurological or musculoskeletal disorder that may affect hand function * Inability to complete ultrasonographic, electrophysiological, functional, or questionnaire assessments

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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

  • Kanuni Sultan Suleyman Education and Research Hospital

    Küçükçekmece, Istanbul, 34307, Turkey (Türkiye)

More trials for these conditions

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