[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pain-shoulder\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pain-shoulder":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,78],{"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":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100473870","slow-and-accelerated-rehabilitation-protocols-100473870",false,"NCT05450510","Slow and Accelerated Rehabilitation Protocols","Effects of Slow and Accelerated Rehabilitation Protocols After Latissimus Dorsi Transfer in Massive, Irreparable Rotator Cuff Tears","Inclusion Criteria:\n\n* being in the age range of 18-65 years\n* being diagnosed with massive, irreparable rotator cuff tears based on magnetic resonance imaging and clinical continuity tests\n* symptoms are unresponsive to conservative care including steroid injections and physiotherapy for at least 6 months\n* having a good command of the Turkish language\n* scoring above 24 in the Mini Mental State Test\n* ≥80% compliance in completing the post-ARCR Phase 1 trainings\n* volunteering to participate in the study\n\nExclusion Criteria:\n\n* diabetes mellitus\n* neurological problems\n* cervical disc herniation\n* visual, verbal, and\u002For cognitive defects (aphasia, unilateral neglect, etc.)\n* systemic inflammatory problems\n* hypermobility, trauma, and\u002For inflammation that could be a contraindication for mobilization\n* former shoulder fractures on the affected side\n* advanced glenohumeral arthritis (Hamada grade 3),\n* deltoid muscle dysfunction,\n* irreparable subscapularis tears,\n* active infection,\n* shoulder stiffness,\n* a history of previous shoulder surgery","ALL","18 Years","65 Years",{"count":20,"type":21},38,"ESTIMATED","INTERVENTIONAL",[24],"NA","Latissimus dorsi transfer is an established treatment option with favorable results in massive, irreparable rotator cuff tears, however, it is controversial if earlier motion is detrimental or beneficial to the postoperative goal of reduced pain and improved clinical outcomes. Therefore, the aim of this study is to compare the effects of slow and accelerated rehabilitation protocols after latissimus dorsi transfer in massive, irreparable rotator cuff tears.",[27,28,29],"Rotator Cuff Injuries","Rotator Cuff Tears","Pain, Shoulder",[27,31,32,33],"tear","pain","shoulder","RECRUITING","2025-03-04",{"date":37,"type":38},"2025-03-06","ACTUAL",{"date":40,"type":38},"2022-04-27",{"date":42,"type":21},"2025-12-27",{"name":44,"class":45},"Hacettepe University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":63,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":46},"100528458","precision-medicine-for-nociception-sngception-and-proprioception-100528458","NCT06161038","Precision Medicine for Nociception, Sngception and Proprioception.","Inclusion Criteria:\n\n1.Cohort A:\n\n(1) Age between 20-100 years old. (2) VAS\\>=30 or VAS\\>=30 at 4 kg pressure (3) Diagnosed as myofascial pain syndrome patients and willing to receive treatment (including LLLT, therapeutic ultrasound, and local dextrose injection therapy) 2. Cohort B:\n\n1. Age between 13-65 years old.\n2. Diagnosed as idiopathic scoliosis The diagnosis of scoliosis was confirmed by antero-posterior plain Xray with Cobbs angle larger than 10 degrees.\n\nExclusion Criteria:\n\n1.Cohort A: Those having active infection, malignancy, and hematological diseases were excluded. The patients had received local injection at upper trapezius within 6 months are also excluded.\n\n2.Cohort B:\n\n1. Those having active infection, malignancy, and hematological diseases were excluded.\n2. Those having specific etiologies of scoliosis, including congenital scoliosis due to malformation or faulty segmentation of the vertebrae and neuromuscular scoliosis due to muscular imbalance, syndromic scoliosis or degenerative scoliosis.\n3. Pregnancy.","13 Years","100 Years",{"count":56,"type":21},160,[24],"Precision medicine is defined as \"an emerging approach for disease treatment and prevention that takes into account individual variability in genes, environment, and lifestyle for each person\" by the Precision Medicine Initiative.\n\nPatients have different response to different treatment modalities, and sore\u002Fpain medicine is no exception. In our experience, low-level laser (LLL), ultrasound, and prolotherapy can reduce sore \u002Fpain through different genetic pathway. Whether the therapeutic effect is controlled by the genetic variants of those sore \u002Fpain related genes or not, is still in debate. The aims of this study are (1) To set up next generation sequencing (NGS)-based approach to find genetic variants which can determine the response of sng\u002Fpain treatment modalities and the phenotype of idiopathic scoliosis. (2) To find possible metabolomics and proteomic markers of sng\u002Fpain. (3) To determine the algorithm of precision medicine for sng\u002Fpain control via the genetic markers.\n\nInvestigators will recruit 80 myofascial pain participant and 80 idiopathic scoliosis participant from Department of Physical Medicine and Rehabilitation, National Taiwan University Hospital Bei-Hu Branch in 2023 and 2025. The myofascial pain participant participants will receive LLL, ultrasound, and prolotherapy, and the therapeutic effect will be recorded. The clinical trial will evaluate the Sng \u002F pain (VAS) and muscle tone of the idiopathic scoliosis participant. The blood and urine samples from the first, the second, and the third visits will be analyzed by next generation sequencing, and mass spectrometry to find the possible biomarker in 2024 and 2025. Investigators expect to develop the individualized treatment plan by means of these biomarkers. Hopefully, the results will be widely applied in the field of sore \u002Fpain medicine.",[60,29,61,62],"Rehabilitation","Pain, Chronic","Idiopathic Scoliosis",[64,65,66,67,68],"Sng \u002F Pain","Precision medicine","Next generation sequencing","Proprioception","Prolotherapy","2024-10-17",{"date":71,"type":38},"2024-10-21",{"date":73,"type":38},"2023-10-01",{"date":75,"type":21},"2025-12-31",{"name":77,"class":45},"National Taiwan University Hospital",{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":85,"targetDuration":87,"studyType":88,"phases":4,"briefSummary":89,"conditions":90,"keywords":93,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":46},"100556936","anterior-shoulder-dislocation-at-emergency-department-100556936","NCT06531590","Anterior Shoulder Dislocation at Emergency Department","Emergency Department Management of Anterior Shoulder Dislocation Patients","Inclusion Criteria:\n\nPatients aged 18 years and older\n\nExclusion Criteria:\n\nPatients who are not conscious at the time of admission and do not consent to participate in the study.\n\nPatients who do not have follow-up in our healthcare system or cannot be followed up.\n\nPatients with allergies to opioids or local anesthetics. Patients presenting to the emergency department with suspicion of multiple fractures and dislocations involving ≥2 different types of injuries will also be excluded from the study.\n\nForensic cases",{"count":86,"type":21},140,"1 Day","OBSERVATIONAL","In this study, investigator will analyze the demographic characteristics of patients presenting to emergency department with Anterior Shoulder Dislocation. Investigators will document the mechanism of injury, orthopedic classification of shoulder dislocation, associated treatments, pre-procedural pain scoring, post-procedural pain scoring, as well as the duration of emergency department stay related to the preferred treatment, orthopedic consultation, and patient outcomes (discharge, admission to ward or intensive care unit, mortality). Aim of the study to investigate whether the current treatments used provide any superiority in emergency department outcomes for patients",[91,92,29],"Shoulder Dislocation","Analgesia",[94,95,96,97,98],"shoulder dislocation","interscalene nerve block","suprascapular nerve block","intraarticular lidocaine injection","emergency department","2024-07-29",{"date":101,"type":38},"2024-08-01",{"date":103,"type":38},"2024-03-01",{"date":105,"type":21},"2026-03-01",{"name":107,"class":45},"Saglik Bilimleri Universitesi"]