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Can magnetic pulses ease nerve pain in the lower back?

NCT ID NCT07743424

Symptom relief Sponsor: Yara Aboelazm Abd Elaziz Mohamed Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 03, 2026 · Last updated Sep 11, 2026 · Updated 2 times

Summary

This trial tests whether adding trans-spinal electromagnetic neuromodulation to standard physical therapy can reduce pain and improve function in people with chronic lumbosacral radiculopathy—a condition where a herniated disc presses on spinal nerves, causing pain, numbness, or weakness in the lower back and leg. About 30 adults aged 20 to 40 with confirmed disc herniation will receive either physical therapy alone or physical therapy plus 15-minute sessions of electromagnetic stimulation on the affected area. Researchers will measure changes in pain, disability, nerve signals, and leg mobility to see if the added treatment makes a meaningful difference.

What this could mean

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

Active substance
Trans-spinal electromagnetic neuromodulation
What this could lead to
If it works, this could offer a non-invasive way to reduce pain and improve mobility for people with nerve-related back and leg pain.
What could go wrong
This is a small early-stage trial, so results may not apply broadly. The treatment's benefits and safety are not yet proven, and it may not outperform standard physical therapy.

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 30 people

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

Started

Sep 2026

Expected to finish

Feb 2027

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

20 to 40 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: 1. patient age range from 20 -40 from both sexes. 2. Unilateral chronic lumbosacral radiculopathy confirmed by neurosurgeon for more than 3 months. 3. Unilateral paracentral or lateral intervertebral disc herniation confirmed by MRI . 4. one of the following: 1. H- reflex amplitude side to side difference 67% in absence of latency difference. 2. H- reflex amplitude side to side difference smaller than 50% in presence of latency difference. c - Side to side H- reflex latency difference more than 1 msec. d- Prolonged H-reflex latency more than 30 msec. Exclusion Criteria: 1. Hypertension 2. Diabetes. 3. Lumbar canal stenosis 4. Pervious surgeries 5. Scoliosis 6. Kyphosis 7. Spinal fracture 8. Bilateral symptoms.

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Conditions

The condition(s) this trial relates to.

radiculopathy

As listed by the trial registrant

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

Discogenic lumbosacral radiculopathy Lumbar radiculopathy

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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.

Contacts and locations

Locations

  • Outpatient Clinic at the Faculty of Physical Therapy Cairo

    RECRUITING

    Giza, Egypt

More trials for these conditions

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