[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"lumbar-spinal-fusion\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:lumbar-spinal-fusion":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,80],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":4},"100622062","back-to-life---early-rehabilitation-therapy-for-patients-undergoing-lumbar-spinal-fusion---a-single-case-experimental-study-100622062",false,"NCT07378735","Back to Life - Early Rehabilitation Therapy for Patients Undergoing Lumbar Spinal Fusion - A Single-case Experimental Study","Back to Life - Early Rehabilitation Therapy for Patients Undergoing Lumbar Spinal Fusion Surgery - A Single-case Experimental Design Study","Back to Life","The investigators will in total include 12 patients undergoing an LSF from the Centre for Rheumatology and Spine Diseases at Rigshospitalet, Denmark.\n\nBefore inclusion, a pilot of three participants will be performed.\n\nInclusion Criteria for all included:\n\n* ≥ 18 years of age\n* Low back pain (LBP) \\> 3 months\n* Read and understand the Danish language\n* The participants should be a part of Frederiksberg Municipality and Copenhagen Municipality (in Denmark)\n\nExclusion Criteria:\n\n* Post-traumatic vertebral compression\u002Fdeformity\n* Patients with the following conditions (infection, neoplasm, metastasis, metabolic bone disease, fractures or other known autoimmune arthropathies)\n* Patients with patient-related circumstances (physical or mental status) that impede their ability to give informed consent and adhere to the study program (e.g., dementia, developmental disorders, or substance-induced cognitive impairment)\n* Other special conditions, where the patient is judged by the surgeon as inappropriate to participate","ALL","18 Years",{"count":20,"type":21},12,"ESTIMATED","INTERVENTIONAL",[24],"NA","Aim This study aims to assess the effectiveness of an early intervention comprising individually tailored physiotherapy, including dialogue, education, and graded activity, following lumbar spinal fusion surgery. The effectiveness will be evaluated on patient-specific goals, physical activity, pain intensity, pain interference, fear of movement, and pain self-efficacy for patients after a lumbar spinal fusion.",[27,28],"Low Back Pain","Lumbar Spinal Fusion",[30,31,32,33,34,35,36,37],"Physical activity","Low back pain","Lumbar spinal fusion","Exercise","Rehabilitation","Physiotherapy","Single-case experimental study","Cognitive behavioural approach","NOT_YET_RECRUITING","2026-01-30",{"date":41,"type":42},"2026-02-03","ACTUAL",{"date":44,"type":21},"2026-02",{"date":46,"type":21},"2028-11",{"name":48,"class":49},"Rigshospitalet, Denmark","OTHER",{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":57,"sex":17,"minAge":18,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":61,"briefSummary":63,"conditions":64,"keywords":65,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":79},"100555524","phase-4-ketorolac-effects-on-post-operative-pain-and-lumbar-fusion-100555524","NCT06513208","Ketorolac Effects on Post-operative Pain and Lumbar Fusion","Ketorolac Effects on Post-operative Pain and Lumbar Fusion: a Double Blind Randomized Controlled Trial","Inclusion Criteria:\n\n* 18-85 years old (inclusive)\n* Elective posterior lumbar instrumented fusion\n* One or two level fusion\n* Consent to participate in study and willing to adhere to study follow up\n* English proficiency\n\nExclusion Criteria:\n\n* \\\u003C 18 or \\> 85 years old\n* History of renal failure, dialysis, or creatinine over 1.50 mg\u002Fdl\n* Active or recent smoker (active within past 6 months)\n* Revision surgery\n* Auto\u002Fworker compensation\n* Active cancer or history of chemotherapy in past 6 months\n* Active narcotic use within 3 months of surgery date\n* Infection at operative levels\n* Any allergies to NSAIDs or Opioids",true,"85 Years",{"count":60,"type":21},140,[62],"PHASE4","A double blind prospective randomized trial of IV ketorolac vs. placebo in management of patients undergoing lumbar one or two level spinal fusions.",[28],[66,67,68],"ketorolac","toradol","lumbar spine fusion","RECRUITING","2025-12-18",{"date":72,"type":42},"2025-12-22",{"date":74,"type":21},"2026-01",{"date":76,"type":21},"2027-06",{"name":78,"class":49},"University of Maryland St. Joseph Medical Center",1,{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":90,"briefSummary":91,"conditions":92,"keywords":93,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":79},"100431935","erector-spinae-plane-block-in-lumbar-spinal-fusion-100431935","NCT04904575","Erector Spinae Plane Block in Lumbar Spinal Fusion","Erector Spinae Plane Block in Lumbar Spinal Fusion : Double-blind, Randomized Controlled Trial.","MERFUSION","Inclusion Criteria:\n\n* Patient with medical insurance.\n* Patient who received information about study and signes a consent to participate in the study.\n* Major patient requiring a lumbar spinal fusion surgery.\n* Patient with an ASA score of 1, 2 or 3.\n\nExclusion Criteria:\n\n* Minor patient.\n* Patient with morphine intolerance\n* Patient with allergy to local anesthetics.\n* Patient consuming morphine for more than 3 months.\n* Pregnant or breastfeeding patient.\n* Patient scheduled for cancer surgery or trauma surgery.\n* Patient participating in another interventional study.\n* Patient with history of lumbar spinal fusion.\n* Patient requiring lumbar surgery without arthrodesis.\n* Patient requiring lumbar surgery with inter-lamar or inter-epineal stabilization.\n* Patient refusing to sign the consent form.\n* Patient for whom it is impossible to give informed information.\n* Patient under the protection of justice, under curatorship or under tutorship.",{"count":89,"type":21},130,[24],"The aim of this study is to observe or not a reduction in the consumption of morphine within 72 hours of the realization of an erector spinae plane block when preparing for a lumbar spinal fusion.",[28],[94,95],"Erector spinae plane block","consumption of morphine","2025-11-21",{"date":98,"type":42},"2025-11-24",{"date":100,"type":42},"2022-01-03",{"date":102,"type":21},"2026-12-31",{"name":104,"class":49},"Clinique Saint Jean, France"]