[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cervical-radicular-pain\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cervical-radicular-pain":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,45,69,96,123],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100650229","45-v-vs-60-v-pulsed-radiofrequency-of-the-cervical-dorsal-root-ganglion-for-cervical-radicular-pain-100650229",false,"NCT07744438","45 V vs 60 V Pulsed Radiofrequency of the Cervical Dorsal Root Ganglion for Cervical Radicular Pain","Does Higher Voltage Improve Outcomes in Cervical Radicular Pain? A Comparison of 45 V and 60 V Pulsed Radiofrequency of the Cervical Dorsal Root Ganglion","Inclusion Criteria:\n\n* Unilateral cervical radicular pain consistent with cervical disc herniation.\n* Pain intensity of ≥6 on the Numerical Rating Scale (NRS).\n* Radicular pain persisting for at least 3 months.\n* MRI evidence of lower cervical nerve root compression consistent with clinical findings.\n* Inadequate response to conservative treatment, including analgesic medications and physical therapy.\n* Completion of cervical dorsal root ganglion pulsed radiofrequency (PRF) treatment.\n\nExclusion Criteria:\n\n* Bilateral upper extremity pain or predominant axial neck pain.\n* Cervical spinal stenosis, spondylolisthesis, cervical myelopathy, or other structural spinal disorders causing radicular pain.\n* Previous cervical spine surgery at the target level.\n* Cognitive impairment preventing reliable outcome assessment.\n* Active local or systemic infection.\n* Coagulopathy or inability to discontinue anticoagulant\u002Fantiplatelet therapy for the procedure.\n* Severe hepatic or renal failure.\n* Pregnancy.\n* Unstable psychiatric disorders.\n* Any condition that could interfere with completion of follow-up evaluations.","ALL","18 Years","65 Years",{"count":20,"type":21},58,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to compare the clinical outcomes of 45 V and 60 V pulsed radiofrequency (PRF) applied to the cervical dorsal root ganglion (DRG) in patients with cervical radicular pain. Treatment efficacy will be evaluated using the Numerical Rating Scale (NRS) for pain intensity and the Neck Disability Index (NDI) for functional disability. Procedure-related adverse events will also be compared to assess the safety of both voltage settings.",[27],"Cervical Radicular Pain",[29,30,31,32],"Pulsed Radiofrequency Treatment","Dorsal Root Ganglion","Voltage","Neck Disability Index","RECRUITING","2026-07-29",{"date":36,"type":37},"2026-08-04","ACTUAL",{"date":34,"type":37},{"date":40,"type":21},"2027-03-01",{"name":42,"class":43},"Ankara Etlik City Hospital","OTHER_GOV",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":68},"100648664","effects-of-myokinetic-stretching-technique-and-post-facilitation-stretching-on-pain-range-of-motion-and-functional-disability-in-patients-with-cervical-radicular-pain-100648664","NCT07724470","Effects of Myokinetic Stretching Technique and Post Facilitation Stretching on Pain, Range of Motion, and Functional Disability in Patients With Cervical Radicular Pain","Inclusion Criteria:\n\n1. Both male and female gender\n2. Age 30 to 60 years with a +ve spurling test and radiating arm pain for more than 4 weeks\n3. Unilateral cervical radicular pain\n4. +ve upper limb tension test and neck disability index \\\u003C50%\n\nExclusion Criteria:\n\n1. History of cervical spinal surgery\n2. Severe facet joint osteoarthritis\n3. History of fracture in the head and neck region\n4. Patient with cognitive dysfunction or mental illness, severe cardiovascular, cerebrovascular, liver, or kidney dysfunction\n5. History of dizziness, vertigo, and vomiting\n6. Osteoporosis and prolonged use of steroids\n7. Cervical myelopathy, tumor, or infectious disease","30 Years","60 Years",{"count":54,"type":21},40,[24],"Cervical radicular pain (CRP) is a musculoskeletal condition characterized by neck pain radiating to the upper limb due to compression or irritation of cervical nerve roots. It significantly affects daily activities, cervical mobility, and overall quality of life. Conventional physical therapy focuses on reducing pain and improving function; however, there is limited evidence comparing the effectiveness of different stretching techniques used in clinical practice.\n\nThis randomized controlled trial aims to compare the effectiveness of Myokinetic Stretching Technique (MST) and Post Facilitation Stretching (PFS) on pain intensity, cervical range of motion, and functional disability in patients with cervical radicular pain.\n\nA total of 70 participants with cervical radicular pain (\\>4 weeks) will be randomly allocated into two groups:\n\nGroup A (Myokinetic Stretching Technique Group) - receiving MST along with conventional therapy including hot pack application, cervical isometric exercises, neurodynamic gliding, and continuous cervical traction.\n\nGroup B (Post Facilitation Stretching Group) - receiving Post Facilitation Stretching along with the same conventional therapy.\n\nThe intervention will be conducted for 4 weeks, with 3 sessions per week on alternate days, each session lasting approximately 45 minutes.\n\nOutcome measures will include:\n\nPain intensity assessed using the Visual Analogue Scale (VAS) Cervical range of motion measured using a goniometer Functional disability assessed using the Neck Disability Index (NDI)\n\nThis study aims to determine the more effective stretching technique for reducing pain, improving cervical mobility, and enhancing functional outcomes, thereby supporting evidence-based physiotherapy practice in managing cervical radicular pain.",[27],"2026-07-21",{"date":60,"type":37},"2026-07-24",{"date":62,"type":37},"2026-06-29",{"date":64,"type":21},"2026-09-15",{"name":66,"class":67},"Lahore University of Biological and Applied Sciences","OTHER",2,{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":76,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":79,"briefSummary":80,"conditions":81,"keywords":82,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":44},"100631862","neuromuscular-re-education-on-pain-rom-and-disability-in-cervical-radiculopathy-100631862","NCT07506200","Neuromuscular Re-education on Pain, ROM and Disability in Cervical Radiculopathy","Effects of Neuromuscular Re-education on Pain, Range of Motion and Disability in Patients With Cervical Radiculopathy","Inclusion Criteria:\n\n* Participants of Age between 30 and 50 years old.\n* Participants of both gender included.\n* Participants having Unilateral upper extremity pain, paresthesia, or numbness\n* Participants with Four positive findings required:\n* Positive Spurling's test\n* Positive distraction test\n* Positive upper limb tension test\n* Ipsilateral cervical rotation less than 60 degrees\n* Participants must have experienced pain for at least 3 months.\n* Participants must have a pain score of 4 to 6 on the 0-10 scale\n\nExclusion Criteria:\n\n* Participants having prior cervical spine surgery.\n* Participants with Cervical vertebral fracture\n* Participants with severe osteoporosis, rheumatic disease, shoulder disease, or infection will be excluded.\n* Participants with vertebro-basilar artery insufficiency and diabetic neuropathy","50 Years",{"count":78,"type":21},52,[24],"This study explores the effectiveness of Neuromuscular Re-education compared to conventional therapies in managing pain, range of motion, and disability in patients with Cervical Radiculopathy",[27],[83,84,85,86],"Cervical Radiculopathy","Neuromuscular Re-education","Range of Motion","Pain Management","2026-06-08",{"date":89,"type":37},"2026-06-10",{"date":91,"type":37},"2026-03-01",{"date":93,"type":21},"2026-07-15",{"name":95,"class":67},"Riphah International University",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":100,"acronym":4,"eligibilityCriteria":101,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":102,"targetDuration":4,"studyType":22,"phases":104,"briefSummary":105,"conditions":106,"keywords":108,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":44},"100616610","investigation-of-the-effects-of-interlaminar-epidural-steroid-injection-on-upper-extremity-proprioception-in-patients-with-chronic-cervical-radiculopathy-100616610","NCT07307846","Investigation of the Effects of Interlaminar Epidural Steroid Injection on Upper Extremity Proprioception in Patients With Chronic Cervical Radiculopathy","Inclusion Criteria:\n\nParticipants must meet all of the following:\n\n* Female or male, 18-65 years of age\n* Presence of unilateral cervical radicular pain lasting at least 3 months\n* MRI of the cervical spine within the last 12 months demonstrating at least one cervical disc herniation consistent with the patient's symptoms\n* Diagnosed with chronic cervical radiculopathy based on history, physical examination, and clinical evaluation\n* Ability to read and write (literacy)\n* Willingness to participate and ability to provide written informed consent\n\nExclusion Criteria:\n\nParticipants will be excluded for any of the following:\n\n* Cervical physical therapy or cervical spinal injection performed within the past 6 months\n* Symptoms or diagnosis of upper extremity entrapment neuropathy\n* Documented vitamin B12 deficiency or vitamin D deficiency on laboratory results within the past year\n* History of cervical spine surgery or significant cervical trauma\n* Bilateral cervical radicular pain\n* Cervical spinal stenosis\n* History of upper extremity surgery or significant upper extremity trauma\n* Cognitive impairment, major psychiatric disorder, intellectual disability, or history of significant neurological disease\n* Diagnosis of polyneuropathy\n* Diagnosis of Diabetes Mellitus\n* Diagnosis of fibromyalgia\n* Current use of medications that may impair proprioception or have sedative effects (e.g., gabapentinoids, antidepressants, muscle relaxants)\n* Active local or systemic infection\n* Coagulopathy or bleeding diathesis\n* Known allergy to any components of the planned injection (triamcinolone, lidocaine, saline, contrast medium)\n* Pregnancy\n* Inability or unwillingness to provide informed consent\n* Illiteracy (unable to read or write)\n\nWithdrawal Criteria\n\n* Voluntary withdrawal of consent at any time\n* Inability or unwillingness to continue study participation for any reason\n* New medical condition or event after enrollment that renders continuation unsafe according to the investigator's judgment",{"count":103,"type":21},46,[24],"Cervical radiculopathy is a common condition caused by irritation or compression of cervical nerve roots, often leading to unilateral neuropathic pain and functional impairment. Proprioceptive deficits in the upper extremity have been demonstrated in various cervical spine disorders; however, the effect of interlaminar epidural steroid injection (ILESI) on upper extremity proprioception in patients with chronic cervical radiculopathy has not been previously examined.\n\nThis prospective interventional study aims to evaluate changes in upper extremity proprioception following unilateral ILESI in patients with cervical disc herniation-related chronic radiculopathy. A secondary aim is to investigate the relationship between proprioceptive changes and clinical outcomes such as pain, neuropathic pain, disability, grip strength, and quality of life.",[83,27,107],"Proprioception",[109,110,111,112,113],"cervical radiculopathy","cervical radicular pain","interlaminar epidural steroid injection","proprioception","proprioceptive impairment","2025-12-31",{"date":116,"type":37},"2026-01-02",{"date":118,"type":21},"2026-01-05",{"date":120,"type":21},"2026-05-01",{"name":122,"class":67},"Marmara University",{"id":124,"slug":125,"hasResults":11,"nctId":126,"briefTitle":127,"officialTitle":128,"acronym":4,"eligibilityCriteria":129,"healthyVolunteers":130,"sex":16,"minAge":17,"maxAge":131,"enrollmentInfo":132,"targetDuration":4,"studyType":22,"phases":134,"briefSummary":135,"conditions":136,"keywords":138,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":141,"lastUpdatePostDateStruct":142,"startDateStruct":144,"completionDateStruct":146,"leadSponsor":148,"locationsCount":44},"100521420","predictors-of-response-to-manual-physiotherapy-using-somatosensory-profiles-in-patients-with-cervicobrachial-pain-100521420","NCT06069362","Predictors of Response to Manual Physiotherapy Using Somatosensory Profiles in Patients With Cervicobrachial Pain","Prediction of Response to Manual Physiotherapy Using Somatosensory Profiles in Patients With Cervicobrachial Pain","Inclusion Criteria:\n\n* Subjects with unilateral cervicobrachial pain\n\nExclusion Criteria:\n\n* Signs of severe disease, cervical myelopathy, tumour, rheumatic diseases or a neurological pathology of central origin.\n* Cervicobrachial pain of traumatic origin or as a result of whiplash.\n* Previous surgical intervention of the cervical spine.",true,"80 Years",{"count":133,"type":21},91,[24],"The goal of this clinical trial is to investigate about the characteristics that predict response to physiotherapy treatment in patients with nerve related neck arm pain. The main question to answer is whether there is a subgroup that responds better to physiotherapy treatment.\n\nParticipants will be assessed for clinical and neurophysiological characteristics prior to treatment. Afterwards they will receive 6 sessions of manual physiotherapy treatment along with home nerve gliding exercises once a week. Baseline measurements will be taken again after treatment to know if there have been any changes.",[27,83,137],"Cervical Pain",[139,140],"Cervicobrachial pain","Nerve related neck arm pain","2025-03-25",{"date":143,"type":37},"2025-03-26",{"date":145,"type":37},"2023-04-20",{"date":147,"type":21},"2025-07-20",{"name":149,"class":67},"University of Deusto"]