[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100650021":3},{"organization":4,"outcomesModule":7,"designInfo":31,"detailedDescription":39,"studyPopulation":30,"armGroups":40,"interventions":53,"overallOfficials":30,"centralContacts":30,"locations":61,"responsibleParty":80,"collaborators":30,"id":84,"slug":85,"hasResults":86,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":30,"eligibilityCriteria":90,"healthyVolunteers":86,"sex":91,"minAge":92,"maxAge":93,"enrollmentInfo":94,"targetDuration":30,"studyType":97,"phases":98,"briefSummary":100,"conditions":101,"keywords":30,"overallStatus":64,"whyStopped":30,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":113},{"fullName":5,"class":6},"Cairo University","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":30,"otherOutcomes":30},[9,13,17,20,24,27],{"measure":10,"description":11,"timeFrame":12},"Pain","Numeric Pain Rating Scale (0-10)","Change from Baseline pain at 6 weeks",{"measure":14,"description":15,"timeFrame":16},"Disability","Oswestry disability index (0-100%)","Change from Baseline disability at 6 weeks",{"measure":18,"description":18,"timeFrame":19},"Straight leg raise test","Change from Baseline straight leg raise test at 6 weeks",{"measure":21,"description":22,"timeFrame":23},"H-reflex side-to-side amplitude (H\u002FH) ratio","by EMG unit","Change from Baseline H-reflex side-to-side amplitude (H\u002FH) ratio at 6 weeks",{"measure":25,"description":22,"timeFrame":26},"Sensory tactile threshold","Change from Baseline Sensory tactile threshold at 6 weeks",{"measure":28,"description":22,"timeFrame":29},"Motor evoked potential","Change from Baseline motor evoked potential at 6 weeks",null,{"allocation":32,"interventionModel":33,"interventionModelDescription":30,"primaryPurpose":34,"observationalModel":30,"timePerspective":30,"maskingInfo":35},"RANDOMIZED","PARALLEL","TREATMENT",{"masking":36,"maskingDescription":30,"whoMasked":37},"SINGLE",[38],"OUTCOMES_ASSESSOR","Patients will be randomized into either Trans-spinal Electromagnetic Neuromodulation group or Conventional physical therapy group. Patients will receive the intervention for six weeks. Outcomes will be assessed at baseline and post-intervention.",[41,48],{"label":42,"type":43,"description":44,"interventionNames":45},"Trans-spinal Electromagnetic Neuromodulation + Conventional physical therapy","EXPERIMENTAL","Patients in this group will receive Trans-spinal Electromagnetic Neuromodulation + Conventional physical therapy",[46,47],"Other: Trans-spinal Electromagnetic Neuromodulation","Other: Conventional physical therapy",{"label":49,"type":50,"description":51,"interventionNames":52},"Conventional physical therapy","ACTIVE_COMPARATOR","Patients in this group will receive Conventional physical therapy",[47],[54,58],{"type":6,"name":55,"description":56,"armGroupLabels":57,"otherNames":30},"Trans-spinal Electromagnetic Neuromodulation","Trans-spinal electromagnetic neuromodulation will be applied for 15 minutes on the affected segment",[42],{"type":6,"name":49,"description":59,"armGroupLabels":60,"otherNames":30},"Conventional physical therapy consisting of:\n\nHot pack on lumbar spine. Neurodynamic mobilization. Rotatory mobilization and rotatory manipulation for lumbar spine. Core stability exercises.",[49,42],[62],{"facility":63,"status":64,"city":65,"state":30,"zip":30,"country":66,"countryCode":67,"cosmosGeoPoint":68,"geoPoint":73,"contacts":74},"Outpatient Clinic at the Faculty of Physical Therapy Cairo","RECRUITING","Giza","Egypt","EG",{"type":69,"coordinates":70},"Point",[71,72],31.20861,30.00944,{"lat":72,"lon":71},[75],{"name":76,"role":77,"phone":78,"phoneExt":30,"email":79},"Yara Aboelazm, MSc","CONTACT","+201008615584","asiaadam135@gmail.com",{"type":81,"investigatorFullName":82,"investigatorTitle":83,"investigatorAffiliation":5,"oldNameTitle":30,"oldOrganization":30},"SPONSOR_INVESTIGATOR","Yara Aboelazm Abd Elaziz Mohamed","MSc","100650021","effect-of-trans-spinal-electromagnetic-neuromodulation-in-treatment-of-patients-with-discogenic-lumbosacral-radiculopathy-100650021",false,"NCT07743424","Effect of Trans-spinal Electromagnetic Neuromodulation in Treatment of Patients With Discogenic Lumbosacral Radiculopathy","Effect of Trans-spinal Electromagnetic Neuromodulation on Pain, Functional Outcome and Motor Evoked Potential in Patients With Discogenic Lumbosacral Radiculopathy","Inclusion Criteria:\n\n1. patient age range from 20 -40 from both sexes.\n2. Unilateral chronic lumbosacral radiculopathy confirmed by neurosurgeon for more than 3 months.\n3. Unilateral paracentral or lateral intervertebral disc herniation confirmed by MRI .\n4. one of the following:\n\n   1. H- reflex amplitude side to side difference 67% in absence of latency difference.\n   2. H- reflex amplitude side to side difference smaller than 50% in presence of latency difference.\n\nc - Side to side H- reflex latency difference more than 1 msec. d- Prolonged H-reflex latency more than 30 msec.\n\nExclusion Criteria:\n\n1. Hypertension\n2. Diabetes.\n3. Lumbar canal stenosis\n4. Pervious surgeries\n5. Scoliosis\n6. Kyphosis\n7. Spinal fracture\n8. Bilateral symptoms.","ALL","20 Years","40 Years",{"count":95,"type":96},30,"ESTIMATED","INTERVENTIONAL",[99],"NA","Purposes of the study\n\nTo investigate the effect of adding Trans-spinal Electromagnetic Neuromodulation to conventional physical therapy in patients with Discogenic Lumbosacral Radiculopathy",[102,103],"Lumbar Radiculopathy","Discogenic Lumbosacral Radiculopathy","2026-09-09",{"date":106,"type":107},"2026-09-11","ACTUAL",{"date":109,"type":107},"2026-09-10",{"date":111,"type":96},"2027-02-10",{"name":82,"class":6},1]