[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"arthrodesis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:arthrodesis":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,55,88,115],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":34,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100648474","evaluation-of-the-effect-of-reiki-on-pain-after-lumbar-surgery-100648474",false,"NCT07722117","Evaluation of the Effect of Reiki on Pain After Lumbar Surgery","Evaluation of the Effect of Reiki on Pain After Lumbar Surgery: A Comparative Randomized, Double-blind, Pilot Study","REDAL","Inclusion Criteria:\n\n* Subject aged 18 years or older.\n* Referred for a lumbar surgery.\n* Absence of participation in another clinical study.\n* Subject affiliated with a social security scheme or beneficiary of such a scheme.\n\nExclusion Criteria:\n\n* Neuropathic patient\n* Presence of neuropathic pain\n* Diagnosis of fibromyalgia\n* Received therapeutic touch, polarity therapy, or professional massage therapy in the past four weeks\n* Unable to undergo medical follow-up for the study\n* Adult subject protected by law, under guardianship or trusteeship",true,"ALL","18 Years",{"count":21,"type":22},60,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial (prospective, comparative, and randomized double-blind study) is to learn if Reiki (a non-pharmacological intervention), when used alongside standard care, can treat and reduce postoperative pain in patients recovering from lumbar surgery (60 participants total, divided into two groups of 30).\n\nThe main questions it aims to answer are:\n\nDoes Reiki significantly reduce postoperative pain levels at day 15 (measured by a Visual Analog Scale) compared to a Sham (placebo) treatment? Does Reiki improve patient quality of life, enhance scar healing, lower daily analgesic consumption, and increase overall patient satisfaction compared to the Sham treatment?\n\nResearchers will compare Group A (30 patients receiving Reiki sessions alongside usual care) to Group B (30 patients receiving Sham\u002Fplacebo sessions alongside usual care) to see if the Reiki group experiences lower pain levels, reduced need for painkillers, better healing, and higher overall satisfaction and quality of life.\n\nParticipants will:\n\n* Receive standard postoperative care following their lumbar surgery.\n* Be randomly assigned to receive either two sessions of actual Reiki therapy or two sessions of a Sham (placebo) treatment.\n* Evaluate their daily pain levels using a Visual Analog Scale (EVA).\n* Complete follow-up assessments at specific intervals (Day 15, Day 21, and Day 30) to track pain levels, pain medication intake, scar healing (using a colorimetric scale), quality of life (via the SF-12 questionnaire), and overall satisfaction (via the Clinical Global Impression scale).",[28,29,30,31,32,33],"The Lumbar Spine Surgical Intervention","Arthrodesis","Severe Herniated Disc","Scoliosis","the Positive Effect of Energy Therapy on Pain Reduction","Alternative to Reduce Analgesic Dependence",[35,36,37,38,39,40,41],"scoliosis","NSAIDs","surgery for lumbar herniated disc","Reiki","energy therapy","the positive effect of energy therapy on pain reduction","alternative to reduce analgesic dependence","RECRUITING","2026-07-23",{"date":45,"type":46},"2026-07-24","ACTUAL",{"date":48,"type":46},"2025-09-10",{"date":50,"type":22},"2028-06",{"name":52,"class":53},"Clinique Bizet","OTHER",2,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":4,"eligibilityCriteria":61,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":62,"targetDuration":64,"studyType":65,"phases":4,"briefSummary":66,"conditions":67,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":87},"100442839","registry-of-arthrex-hand-and-wrist-products-100442839","NCT05046600","Registry of Arthrex Hand and Wrist Products","Multi-Center, Prospective Registry to Evaluate the Continued Safety and Effectiveness of Hand and Wrist Products","Inclusion Criteria:\n\n1. Subject requires surgery using Arthrex hand and wrist implants included in the registry.\n2. Subject is 18 years of age or over.\n3. Subject is not considered a vulnerable subject (i.e. child, pregnant, nursing, prisoner, or ward of the state).\n4. Subject signed informed consent and is willing and able to comply with all registry requirements\n\nExclusion Criteria:\n\n1. Insufficient quantity or quality of bone.\n2. Blood supply limitations and previous infections, which may retard healing.\n3. Foreign-body sensitivity or foreign-body reactions.\n4. Any active infection or blood supply limitations.\n5. Conditions that tend to limit the patient's ability or willingness to restrict activities or follow directions during the healing period.\n6. Subjects that are skeletally immature -",{"count":63,"type":22},650,"12 Months","OBSERVATIONAL","A Multi-Center, Prospective Registry to Evaluate the Continued Safety and Effectiveness of Hand and Wrist Products",[68,69,70,71,72,73,74,29,75,76],"Ulnar\u002FRadial Collateral Ligament Reconstruction","Ligament Repair or Reconstruction","Small Bone Fragments and Arthrodesis","Scapholunate Ligament Reconstruction","Carpal Fusion (Arthrodesis) of the Hand","Digital Tendon Transfers","Carpometacarpal Joint Arthroplasty","Digital Tendon Transfer","Distal Radius Fracture Fixation","2025-06-23",{"date":79,"type":46},"2025-06-26",{"date":81,"type":46},"2021-07-20",{"date":83,"type":22},"2025-12-01",{"name":85,"class":86},"Arthrex, Inc.","INDUSTRY",5,{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":92,"acronym":4,"eligibilityCriteria":93,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":94,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":96,"conditions":97,"keywords":100,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":54},"100586581","wrist-and-carpal-arthrodeses-a-1-year-follow-up-study-100586581","NCT06917235","Wrist and Carpal Arthrodeses. A 1-year Follow-up Study.","Inclusion Criteria:\n\n* All patients undergoing wrist or carpal arthrodesis, regardless of the specific technique.\n* Advanced degenerative changes unresponsive to conservative treatment.\n\nExclusion Criteria:\n\n* Patients who do not accept participation in the study",{"count":95,"type":22},20,"This study at the Orthopedic Department, Drammen Hospital, examines the effectiveness and safety of various arthrodesis procedures in the wrist and carpus to relieve chronic pain and restore functional stability. Arthrodesis, which fuses two or more bones to eliminate joint mobility, is considered as a last resort when conservative treatments do not produce the desired results. The study includes patients with advanced degenerative changes, rheumatoid arthritis, or extensive injuries. Patients assessed preoperatively and postoperatively through measurements of range of motion, grip strength, and pain using various tools such as PRWHE, QuickDASH, EQ-5D-5L and NRS. The checks include X-rays and CT to evaluate healing. The data is analyzed to identify trends and factors that influence positively outcome. The follow-up takes place after 8 weeks, 3 months and 1 year postoperatively, with a focus on pain relief and functional improvement. The data are compared before and after surgery to assess the effectiveness of the intervention efficiency. The study has been applied for approval by REK, but rejected because it was assessed as a quality control project, and applied for the Data Protection Commissioner (PVO).\n\nThe data is anonymised and stored on secure servers, with switch keys stored separately. The patients give informed consent and are insured through Norwegian Patient Injury Compensation. The study seeks to improve patient care by increasing understanding of the long-term effects of osteoarthritis, including complications and secondary osteoarthritis. The results will contribute to better clinical decisions and treatments.",[29,98,99],"Arthrosis","Wrist Osteoarthritis",[101,102,103,104,105],"Wrist arthrodesis","carpal arthrodesis","follow-up","surgery","fusion","2025-04-09",{"date":108,"type":46},"2025-04-13",{"date":110,"type":46},"2024-09-01",{"date":112,"type":22},"2029-08-15",{"name":114,"class":53},"Vestre Viken Hospital Trust",{"id":116,"slug":117,"hasResults":11,"nctId":118,"briefTitle":119,"officialTitle":120,"acronym":121,"eligibilityCriteria":122,"healthyVolunteers":11,"sex":18,"minAge":123,"maxAge":124,"enrollmentInfo":125,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":127,"conditions":128,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":139},"100450456","instrumented-posterolateral-arthrodesis-for-adolescent-idiopathic-scoliosis-100450456","NCT05145725","Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic Scoliosis","Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic Scoliosis: Observational Study","APOSIA","Inclusion Criteria:\n\n* Patient between 12 and 20 years old\n* Scoliosis in adolescents for whom surgery has been proposed based on radiological criteria (Cobb angle\\> 25 ° for thoracolumbar and lumbar scoliosis,\\> 35 ° for thoracic scoliosis and\\> 40 ° for double major scoliosis)\n* Patient affiliated or beneficiary of a social security scheme or attached to a beneficiary of a social security scheme\n* Patient and legal representative having been informed and not opposing this research\n\nExclusion Criteria:\n\n* Patient over 20 years old\n* Non-surgical scoliosis\n* Refusal to participate in the study by the child or parents","12 Years","20 Years",{"count":126,"type":22},866,"The study population concerns adolescent patients with idiopathic scoliosis which requires surgical management and who have a longer waiting period of 6 months.\n\nThe aim of this study is to research the predictive factors of an improvement in the quality of life of adolescents who have had surgery.",[129,29],"Scoliosis; Adolescence","2024-02-28",{"date":132,"type":46},"2024-02-29",{"date":134,"type":46},"2021-03-18",{"date":136,"type":22},"2036-03-18",{"name":138,"class":53},"Elsan",1]