Not Yet RecruitingNot Applicable

Effect of Trans-spinal Electromagnetic Neuromodulation in Treatment of Patients With Discogenic Lumbosacral Radiculopathy

Egypt30 participantsStarted 2026-08-01

Plain-language summary

Purposes of the study To investigate the effect of adding Trans-spinal Electromagnetic Neuromodulation to conventional physical therapy in patients with Discogenic Lumbosacral Radiculopathy

Who can participate

Age range

20 Years – 40 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. patient age range from 20 -40 from both sexes.
. Unilateral chronic lumbosacral radiculopathy confirmed by neurosurgeon for more than 3 months.
. Unilateral paracentral or lateral intervertebral disc herniation confirmed by MRI .
. one of the following:
. H- reflex amplitude side to side difference 67% in absence of latency difference.
. H- reflex amplitude side to side difference smaller than 50% in presence of latency difference.

Exclusion criteria

. Hypertension
. Diabetes.
. Lumbar canal stenosis
. Pervious surgeries
. Scoliosis
. Kyphosis

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Pain

Timeframe: Change from Baseline pain at 6 weeks

Disability

Timeframe: Change from Baseline disability at 6 weeks

Straight leg raise test

Timeframe: Change from Baseline straight leg raise test at 6 weeks

H-reflex side-to-side amplitude (H/H) ratio

Timeframe: Change from Baseline H-reflex side-to-side amplitude (H/H) ratio at 6 weeks

Sensory tactile threshold

Timeframe: Change from Baseline Sensory tactile threshold at 6 weeks

Motor evoked potential

Timeframe: Change from Baseline motor evoked potential at 6 weeks

Trial details

NCT IDNCT07743424

SponsorYara Aboelazm Abd Elaziz Mohamed

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-08-01

View on ClinicalTrials.gov More Lumbar Radiculopathy trials