[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"lumbar-surgery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:lumbar-surgery":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,53,81],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":33,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100618643","retrolaminar-analgesia-for-lumbar-surgery-100618643",false,"NCT07334288","Retrolaminar Analgesia for LuMbar Surgery","Efficacy of Ultrasound-Guided Retrolaminar Block Combined With Standard Multimodal Analgesia for Postoperative Pain Management in Lumbar Spine Surgery: A Randomized Controlled Trial","REALM","Inclusion Criteria:\n\n* Adult patients aged 18-80 years\n* Scheduled for elective lumbar spine surgery (with instrumentation)\n* American Society of Anesthesiologists (ASA) physical status I-III\n* Willing and able to provide written informed consent\n* Able to use patient-controlled analgesia (PCA) device\n\nExclusion Criteria:\n\n* Refusal to participate in the study\n* Known allergy to local anesthetics (bupivacaine - levobupivacaine - lidocaine) or any study medication\n* Contraindication to regional anesthesia (infection at injection site, coagulopathy)\n* Chronic opioid use (daily use for \\>3 months prior to surgery)\n* Severe psychiatric disorder that precludes informed consent\n* Emergency surgery\n* Diabetes mellitus with preoperative glucose \\>180 mg\u002Fdl\n* Pregnancy or breastfeeding\n* Body mass index (BMI) \\>40 kg\u002Fm²\n* Reoperation or revision of the same level of previous spinal surgery","ALL","18 Years","80 Years",{"count":21,"type":22},50,"ESTIMATED","INTERVENTIONAL",[25],"NA","This randomized controlled trial evaluates the effectiveness of ultrasound-guided retrolaminar nerve block in addition to standard multimodal analgesia for postoperative pain management in patients undergoing lumbar spine surgery. Fifty patients will be randomly assigned to receive either the retrolaminar block combined with standard pain management or standard pain management alone. The primary outcome is total opioid consumption in the first 24 hours after surgery. Secondary outcomes include pain intensity at multiple time points, time to first rescue analgesia, duration of sensory block, incidence of postoperative nausea and vomiting, length of hospital stay, patient satisfaction, and chronic pain development at 3 and 6 months follow-up.",[28,29,30,31,32],"Postoperative Pain","Lumbar Surgery","Back Pain Lower Back Chronic","Opioid Analgesia","Regional Anaesthesia",[34,35,36,37,38,39],"retrolaminar block","regional anesthesia","lumbar spine surgery","Multimodal analgesia","opioid consumption","Ultrasound-guided nerve block","RECRUITING","2026-04-10",{"date":43,"type":44},"2026-04-13","ACTUAL",{"date":46,"type":44},"2026-03-01",{"date":48,"type":22},"2027-06-01",{"name":50,"class":51},"Universidad de los Andes, Chile","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":23,"phases":61,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":52},"100610744","the-effect-of-mobilization-training-given-to-patients-undergoing-lumbar-stabilization-surgery-on-postoperative-pain-anxiety-kinesiophobia-fear-of-falling-and-mobility-100610744","NCT07231562","The Effect of Mobilization Training Given to Patients Undergoing Lumbar Stabilization Surgery on Postoperative Pain, Anxiety, Kinesiophobia, Fear of Falling, and Mobility","İnclusion Criteria\n\n* The patient must be over 18 years of age\n* Participate in the study voluntarily,\n* Be undergoing lumbar surgery for the first time\n* Be undergoing lumbar stabilization surgery\n* Be oriented to person, place, and time\n* Not have taken any oral or parenteral analgesic medication other than the routine treatment ordered before mobilization\n* Have no restrictions (physical disability, etc.) that would prevent mobilization,\n* Be able to understand and speak Turkish\n* Have no vision or hearing problems,\n* Have no psychiatric illness, ağrı var\n* Be in ASA 1 or 2,\n* Patients planned to be included in the intervention and control groups must not be in the same rooms.\n\nExclusion Criteria\n\n* Having a neurological (such as dementia\u002FAlzheimer's) or psychiatric (such as schizophrenia) medical diagnosis that affects cognitive status.\n* Having a chronic pain disorder.",{"count":60,"type":22},60,[25],"In this study, the researcher will examine the effects of preoperative mobilization training (video viewing with VR glasses and brochure methods) given to patients undergoing surgery in the lumbar region on pain, anxiety, fear of movement, fear of falling, and mobility levels in the postoperative period, using specific scales.",[64,29],"Lumbar Disease",[66,67,68,69,70],"Lumbar region","kinesiophobia","mobilization","nursing care and education","perioperative period","NOT_YET_RECRUITING","2025-11-14",{"date":74,"type":44},"2025-11-17",{"date":76,"type":22},"2025-11",{"date":78,"type":22},"2026-07",{"name":80,"class":51},"Suleyman Demirel University",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":88,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":89,"targetDuration":91,"studyType":92,"phases":4,"briefSummary":93,"conditions":94,"keywords":98,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":105,"leadSponsor":107,"locationsCount":52},"100599170","myocardial-injury-after-noncardiac-surgery-mins-in-lumbar-surgery-patients-100599170","NCT07081009","Myocardial Injury After Noncardiac Surgery (MINS) in Lumbar Surgery Patients","Evaluation of the Incidence and Risk Factors of Myocardial Injury After Noncardiac Surgery (MINS) in Lumbar Surgery Patients","Inclusion criteria Age ≥18 years Elective lumbar stabilization surgery\n\nExclusion criteria History of cardiac surgery Recent acute MI (\\\u003C30 days) Chronic elevated troponin levels",true,{"count":90,"type":22},180,"270 Days","OBSERVATIONAL","The aim of this study is to evaluate the incidence of myocardial injury after noncardiac surgery (MINS) in patients undergoing lumbar surgery, and to investigate the associated risk factors.",[95,96,29,97],"MYOCARD INFARCTUS","Non Cardiac Surgery","Anesthesia",[99,100],"Myocardial injury","noncardiac surgery","2025-10-01",{"date":103,"type":44},"2025-10-06",{"date":101,"type":44},{"date":106,"type":22},"2026-04-24",{"name":108,"class":51},"Ankara City Hospital Bilkent"]