NCT07743424

Brief 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

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
6mo left

Started Aug 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress6%
Aug 2026Jan 2027

First Submitted

Initial submission to the registry

July 29, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

August 1, 2026

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 3, 2026

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2027

Expected
Last Updated

August 3, 2026

Status Verified

July 1, 2026

Enrollment Period

Same day

First QC Date

July 29, 2026

Last Update Submit

July 29, 2026

Conditions

Outcome Measures

Primary Outcomes (6)

  • Pain

    Numeric Pain Rating Scale (NPRS)

    Change from Baseline pain at 6 weeks

  • Disability

    Oswestry disability index

    Change from Baseline disability at 6 weeks

  • Straight leg raise test

    Straight leg raise test

    Change from Baseline straight leg raise test at 6 weeks

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

    by EMG unit

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

  • Sensory tactile threshold

    by EMG unit

    Change from Baseline Sensory tactile threshold at 6 weeks

  • Motor evoked potential

    by EMG unit

    Change from Baseline motor evoked potential at 6 weeks

Study Arms (2)

Trans-spinal Electromagnetic Neuromodulation + Conventional physical therapy

EXPERIMENTAL

Patients in this group will receive Trans-spinal Electromagnetic Neuromodulation + Conventional physical therapy

Other: Trans-spinal Electromagnetic NeuromodulationOther: Conventional physical therapy

Conventional physical therapy

ACTIVE COMPARATOR

Patients in this group will receive Conventional physical therapy

Other: Conventional physical therapy

Interventions

Trans-spinal electromagnetic neuromodulation will be applied for 15 minutes on the affected segment

Trans-spinal Electromagnetic Neuromodulation + Conventional physical therapy

Conventional physical therapy consisting of: Hot pack on lumbar spine. Neurodynamic mobilization. Rotatory mobilization and rotatory manipulation for lumbar spine. Core stability exercises.

Conventional physical therapyTrans-spinal Electromagnetic Neuromodulation + Conventional physical therapy

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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.
  • c - Side to side H- reflex latency difference more than 1 msec. d- Prolonged H-reflex latency more than 30 msec.

You may not qualify if:

  • Hypertension
  • Diabetes.
  • Lumbar canal stenosis
  • Pervious surgeries
  • Scoliosis
  • Kyphosis
  • Spinal fracture
  • Bilateral symptoms.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Outpatient Clinic at the Faculty of Physical Therapy Cairo

Giza, Egypt

Location

MeSH Terms

Conditions

Radiculopathy

Condition Hierarchy (Ancestors)

Peripheral Nervous System DiseasesNeuromuscular DiseasesNervous System Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
MSc

Study Record Dates

First Submitted

July 29, 2026

First Posted

August 3, 2026

Study Start

August 1, 2026

Primary Completion

August 1, 2026

Study Completion (Estimated)

January 30, 2027

Last Updated

August 3, 2026

Record last verified: 2026-07

Locations