[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"spinal-stenosis-cervical\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:spinal-stenosis-cervical":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,73],{"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":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100632243","does-the-cervical-stenosis-affect-hand-function-100632243",false,"NCT07511153","Does the Cervical Stenosis Affect Hand Function?","Does the Degree of Cervical Spinal Stenosis Affect Hand Function?","Inclusion Criteria:\n\n* Individuals aged 18-75\n* Individuals who have previously undergone a cervical MRI\n* Cases where the degree of stenosis can be clearly determined on MRI\n* Individuals who have had neck pain for at least 3 months\n\nExclusion Criteria:\n\n* Individuals who declined to participate in the study\n* Individuals who had undergone cervical surgery\n* Individuals diagnosed with vertigo\n* Individuals with sudden hearing loss\n* Individuals with additional neurological conditions\n* Individuals with psychiatric or cognitive disorders that would prevent measurement in the study","ALL","18 Years","75 Years",{"count":20,"type":21},180,"ESTIMATED","1 Day","OBSERVATIONAL","The cervical spine is a complex structure that supports the weight of the head and protects the spinal cord and nerve roots. Cervical spinal stenosis (CSS), which develops as a result of degenerative processes, can cause narrowing of the spinal canal and compression of nerve structures, leading to symptoms such as pain, numbness, and weakness. This condition can negatively affect hand function, particularly grip strength and dexterity. However, studies in the literature examining the effect of CSS on grip strength and hand function are limited. Therefore, this study will be conducted to determine the effect of the severity of cervical spinal stenosis, identified in patients who underwent MRI following their presentation with cervical problems at the Physical Medicine and Rehabilitation outpatient clinic of Buca Seyfi Demirsoy Training and Research Hospital, İzmir Democracy University, on hand grip strength and functionality. Grip strength will be assessed using the Jamar hand dynamometer, and fine pinch strength will be evaluated using the Lafayette pinch meter. Additionally, hand functionality will be measured using the Nine-Hole Peg Test. The impact of neck pain on daily life will be assessed using the Neck Disability Index. The data obtained will be compared and analyzed using appropriate statistical methods.\n\nThis study is expected to fill a significant gap in the current literature by comprehensively elucidating the effects of cervical stenosis on hand function and grip performance, thereby contributing to the individualization of rehabilitation approaches.",[26,27,28],"Spinal Stenosis Cervical","Hand Grip Strength","Neck Pain",[30,31,32],"cervical spinal stenosis","hand grip strength","neck pain","NOT_YET_RECRUITING","2026-05-13",{"date":36,"type":37},"2026-05-15","ACTUAL",{"date":39,"type":21},"2026-09-01",{"date":41,"type":21},"2027-12-01",{"name":43,"class":44},"Izmir Democracy University","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":55,"conditions":56,"keywords":57,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":72},"100584243","multicentric-case-series-of-uniportal-endoscopic-posterior-cervical-decompression-for-cervical-spinal-stenosis-100584243","NCT06886802","Multicentric Case Series of Uniportal Endoscopic Posterior Cervical Decompression for Cervical Spinal Stenosis","DEC-SCM","Inclusion Criteria:\n\n* Provision of informed consent to participate in the study.\n* Patients with cervical canal stenosis grade I-III according to the Kang scale.\n* Radicular or myelopathic symptoms.\n* Having undergone complete conservative management, including physical therapy and analgesia, for at least 3 months.\n* Patients who have opted for posterior uniportal endoscopic cervical decompression for cervical canal stenosis.\n\nExclusion Criteria:\n\n* Inability to read or write.\n* Prior cervical surgeries at the levels to be treated.\n* Infectious symptoms or concomitant rheumatologic diseases.\n* Criteria of cervical vertebral instability.\n* Congenital spinal malformations.\n* Disc herniation at the same cervical level to be operated on.\n* Medullary hyperintensity on T2-weighted magnetic resonance imaging in the level(s) to be treated.","74 Years",{"count":54,"type":21},50,"Cervical spinal stenosis is a condition that can cause pain, sensory disturbances, and motor deficits due to the compression of neural structures in the cervical spine. While conservative treatments such as physical therapy and pain management can help some patients, others with persistent neurological deficits may require surgical intervention. Traditional surgical approaches, including anterior decompression and posterior open surgery, have proven effective but carry risks such as vascular or nerve injuries and postoperative pain.\n\nThis study evaluates a minimally invasive surgical approach called Posterior Uniportal Endoscopic Cervical Decompression as an alternative to traditional methods for patients with cervical spinal stenosis. The main objective is to assess changes in neurological deficits and disability related to cervical pain following this procedure. The study will also document hospitalization duration, surgical time, blood loss, and the incidence of postoperative complications.\n\nThis multicenter, prospective case series will recruit 50 patients from three medical centers in Mexico. Participants must have symptomatic cervical spinal stenosis that persists despite at least three months of conservative treatment. Eligible patients will undergo Posterior Uniportal Endoscopic Cervical Decompression, a technique that allows precise nerve decompression through a small incision, minimizing damage to surrounding tissues. Standardized clinical assessment tools, including the modified Japanese Orthopaedic Association (mJOA) scale, Neck Disability Index (NDI), and Visual Analog Scale (VAS) for pain, will be used to evaluate outcomes at multiple time points over 12 months.\n\nBy comparing patients' preoperative and postoperative evaluations, the study aims to determine whether Posterior Uniportal Endoscopic Cervical Decompression effectively improves neurological function and reduces disability while maintaining a favorable safety profile. Findings from this study could support the adoption of minimally invasive endoscopic techniques as a viable option for treating cervical spinal stenosis, potentially leading to faster recovery times and reduced surgical complications compared to traditional methods.",[26],[58,59,60,61],"Cervical Spinal Stenosis","► Minimally Invasive Surgical Procedures","► Endoscopic Spine Surgery","► Spinal Degenerative Disease","RECRUITING","2026-03-03",{"date":65,"type":37},"2026-03-04",{"date":67,"type":37},"2026-02-18",{"date":69,"type":21},"2027-02",{"name":71,"class":44},"TecSalud Investigación Clínica",1,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":82,"conditions":83,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":72},"100611850","assessing-safety-of-cervical-spine-fusion-with-nmp-100611850","NCT07245940","Assessing Safety of Cervical Spine Fusion With NMP®","Assessing Safety of Cervical Spine Fusion With NMP® Graft Material: A Retrospective Chart Review","Inclusion Criteria:\n\n1. Patients treated with NMP® for Cervical (C2-T1) Interbody fusion (2022-2025) at the study site.\n2. Minimum of 90-day post-operative follow up data available\n\nExclusion Criteria:\n\n* Patients with no follow-up data within 3 months from the surgery date due to missed postoperative appointments.",{"count":81,"type":21},300,"The goal of this retrospective chart review study is to assess safety of NMP® in the treatment of cervical spine degenerative conditions by assessing the incidence and nature of AEs in follow-up (minimum of 90 days and up to 2 year post-operatively) as well as reoperation rates.",[84,85,26],"Degenerative Disc Disease","Degenerative Spondylolisthesis","2025-11-17",{"date":88,"type":37},"2025-11-24",{"date":90,"type":21},"2026-01-15",{"date":92,"type":21},"2026-08-01",{"name":94,"class":95},"Red Rock Regeneration Inc.","INDUSTRY"]