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Shock waves vs lasers: which eases Burn-Related nerve pain better?

NCT ID NCT07102992

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This study tested two non-invasive treatments—high-intensity laser therapy and shock wave therapy—for people with cubital tunnel syndrome after an arm burn. 75 adults with healed burns and confirmed ulnar nerve problems received either laser or shock wave therapy plus nerve gliding exercises. The goal was to see which approach better improved nerve function and arm disability over 12 weeks.

What this could mean

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

Active substance
high-intensity laser therapy and extracorporeal shock wave therapy
What this could lead to
If successful, this could point toward a non-invasive treatment option to improve nerve function and arm use after burn-related cubital tunnel syndrome.
What could go wrong
This is a small, completed trial with 75 participants, so results may not apply to everyone. The therapies are compared as add-ons to exercises, and their standalone benefit is unclear.

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

75 people

The number who actually took part.

Started

Aug 2025

Finished

Jun 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

20 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 * Men and women aged 20-50 years. * Healed unilateral second- or third-degree upper-limb burns involving the elbow with a total body surface area (TBSA) \<20%. * Unilateral post-burn cubital tunnel syndrome confirmed clinically (including Tinel's sign) and electrophysiologically by focal slowing of ulnar nerve conduction across the elbow. * Ability and willingness to provide informed consent and comply with the study protocol. Exclusion Criteria * Severe axonal loss indicating direct ulnar nerve injury. * Generalized neuropathy or abnormal nerve conduction in the contralateral upper limb. * Concurrent median or radial neuropathy or brachial plexus injury. * Previous elbow fracture, ulnar nerve surgery, or extensive reconstructive procedures around the cubital tunnel (simple skin grafting permitted). * Diabetes mellitus, active malignancy, pregnancy, active infection, coagulopathy, or cardiac pacemaker implantation. * Other neurological disorders affecting upper-limb function. * Participation in another rehabilitation or interventional study during the study period. * Inability to adhere to the treatment protocol or scheduled 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

  • Out patient clinic , faculty of Physical Therapy, ahram Canadian university

    Giza, Giza Governorate, Egypt