Does nerve healing keep pace with hand recovery after carpal tunnel surgery?
NCT ID NCT07803939
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 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: * 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.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Carpal tunnel syndrome (CTS) are added.
By submitting, you agree to our Terms of use
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can carpal tunnel surgery restore more than hand function?
- Retraining the brain to ease carpal tunnel pain: a new approach put to the test
- Can a Two-Session acupuncture treatment match ten sessions for carpal tunnel?
- Light therapy may soothe wrist pain without surgery
- Nerve glides: a Drug-Free path to ease carpal tunnel pain?
- Can sound waves or nerve glides ease carpal tunnel pain?