[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"arthropathy-shoulder\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:arthropathy-shoulder":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,44,73,95],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100396979","scapular-positioning-in-standing-position-using-sonography-100396979",false,"NCT04449146","Scapular Positioning in Standing Position Using Sonography","3S","Inclusion Criteria:\n\n* Major patients and agreeing to participate in the study after oral and written information.\n* Care course patients for a reverse shoulder arthroplasty on a native shoulder joint\n\nExclusion Criteria:\n\n* Patients under the age of 18\n* Patients refusing to participate in the study\n* Patients whose condition does not allow informed consent\n* Patients who are subject to legal protection (safeguarding of Justice, curatorship, guardianship), persons deprived of their liberty\n* Unaffiliated patients and non-beneficiaries of a health insurance plan","ALL","18 Years","99 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","The objective of this study is to analyse the positioning of the scapula in standing position and compared to the supine position (CT scan) in 3 dimensions (3 rotations of the scapula) using a non-radiant, portable system, combining an ultrasound probe with marker and a camera integrated into a Tablet for the three-dimensional location of the marker (probe).",[27,28],"Shoulder Osteoarthritis","Arthropathy Shoulder",[30],"Reverse Shoulder Arthroplasty","RECRUITING","2026-06-25",{"date":34,"type":35},"2026-06-29","ACTUAL",{"date":37,"type":35},"2022-08-31",{"date":39,"type":21},"2026-08-31",{"name":41,"class":42},"University Hospital, Brest","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":69,"leadSponsor":71,"locationsCount":43},"100574082","phase-4-cora-q15-continuous-vs-single-injection-interscalene-block-on-qor-15-in-outpatient-rotator-cuff-surgery-100574082","NCT06754657","CORA-Q15: Continuous vs. Single-injection Interscalene Block on QoR-15 in Outpatient Rotator Cuff Surgery","Comparison of Continuous vs. Single-injection Interscalene Block on QoR-15 in Outpatient Rotator Cuff Surgery: A Randomized Study Assessing Non-inferiority and Superiority (CORA-Q15)","CORA-Q15","Inclusion Criteria:\n\n* Adults (≥18 years, \\\u003C 75 years) scheduled for elective outpatient arthroscopic rotator cuff repair surgery.\n* Patients capable of managing a continuous outpatient regional analgesia system based on an interscalene block (eligibility criteria: able to understand verbal and written instructions, have home support, and live geographically close to the healthcare center).\n* Willing and able to provide informed, written consent to participate in the study.\n\nExclusion Criteria:\n\n* History of chronic opioid use (\\>3 months).\n* Severe comorbidities (e.g., renal or hepatic failure, ASA classification of 3 or higher).\n* Allergy to local anesthetics, dexamethasone, or the analgesic drugs used in the study.\n* Patients with contraindications for peripheral nerve block.","75 Years",{"count":54,"type":21},150,[56],"PHASE4","The purpose of the study will be to compare the efficacy of single-injection interscalene block versus continuous interscalene block on the quality of recovery in patients undergoing outpatient arthroscopic rotator cuff repair surgery.\n\nThe participants will:\n\n* Be randomized to receive either a single-injection interscalene block or continuous infusion via an elastomeric pump.\n* Be monitored via telephone by the research team to complete the QoR-15 survey, assess pain levels, the need for tramadol use, and any complications.\n* Have follow-up by the Acute Pain Unit during the first 3 days.",[28,59,60],"Pain, Acute","Anesthesia",[62,63,64],"ambulatory surgery","rotator cuff repair","regional anesthesia","2025-05-26",{"date":67,"type":35},"2025-05-30",{"date":65,"type":35},{"date":70,"type":21},"2027-03-31",{"name":72,"class":42},"Pontificia Universidad Catolica de Chile",{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":81,"targetDuration":4,"studyType":22,"phases":83,"briefSummary":84,"conditions":85,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":43},"100583562","determination-of-scapulothoracic-and-glenohumeral-angles-by-imaging-in-patients-after-shoulder-arthroplasty-scap-imag-100583562","NCT06877936","Determination of Scapulothoracic and Glenohumeral Angles by Imaging in Patients After Shoulder Arthroplasty (SCAP-imag)","Determination of Scapulothoracic and Glenohumeral Angles by Imaging in Patients After Shoulder Arthroplasty","SCAP-imag","Inclusion Criteria:\n\n* Major\n* Reverse total shoulder arthroplasty surgery performed by Dr. Lionel Neyton (Jean Mermoz Private Hospital,69008 Lyon) 24±3 months prior to inclusion in the study.\n* Have had a CT scan of the operated shoulder prior to the operation\n* Patient having signed informed consent\n* Patient affiliated to a social security scheme or beneficiary of such a scheme, according to Article L.1124-1 of the Public Health Code\n\nExclusion Criteria:\n\n* Contraindication to the EOS® examination\n* Anthropometry incompatible with the production of EOS images\n* Pregnant, parturient, breastfeeding women\n* Have a history of fracture at the level of the humerus, scapula or clavicle\n* Have a history of surgery on the shoulder or contralateral upper limb to the limb with the prosthesis\n* Protected patient: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision",{"count":82,"type":21},25,[24],"The shoulder is a site particularly affected by osteoarthritis since it affects up to 7% of the population aged over 65. To deal with osteoarthritis, total shoulder prosthesis is an increasingly used solution. Among the different types of total shoulder prostheses, the majority of surgical procedures involve the use of a reverse total shoulder prosthesis. This type of prosthesis modifies the anatomy of the shoulder in order to ensure better stability and mobility of the shoulder in patients while also compensating for potential significant lesions of certain deep muscles of the shoulder joint (i.e., rotator cuff).\n\nReverse prostheses have good short-term results but these are impaired in longer term with a Constant functional score of around 70% at 10 years and a survival rate of 70% after 20 years. Problems of bone conflicts between the scapula and the humerus can also be observed on these reverse total shoulder prostheses with variable rates from 4.6% to 47.3% depending on the position of the prosthesis.\n\nIn order to minimize the risk of complications, several tools are available to surgeons to optimize the positioning of the prosthesis. Planning software can be used to plan the kinematics of the shoulder after arthroplasty and quantify shoulder movements by 1\u002F estimating the scapulothoracic and glenohumeral angles, and 2\u002F determining the scapulohumeral rhythm (i.e., joint coordination index evaluating the relative contribution of these two joints to the total elevation of the arm). This prediction allows the surgeon to adapt the size, shape and position of the implants to each patient in order to ensure optimal shoulder kinematics, namely a maximum amplitude without bone conflicts (contacts) between the scapula and the humerus.\n\nThe main objective of this study is to evaluate the influence of a reverse shoulder arthroplasty on shoulder kinematics at 2 years postoperatively in comparison with the non-operated contralateral limb.",[28],"2025-03-10",{"date":88,"type":35},"2025-03-14",{"date":90,"type":35},"2025-01-29",{"date":92,"type":21},"2027-02-28",{"name":94,"class":42},"Ramsay Générale de Santé",{"id":96,"slug":97,"hasResults":11,"nctId":98,"briefTitle":99,"officialTitle":100,"acronym":4,"eligibilityCriteria":101,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":102,"targetDuration":4,"studyType":104,"phases":4,"briefSummary":105,"conditions":106,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":118},"100555420","fh-ortho-shoulder-observatory-100555420","NCT06511856","FH ORTHO Shoulder Observatory","Observational Study of Shoulder Surgery Using FH ORTHO Medical Devices","Inclusion criteria:\n\n1. Any patient undergoing implantation of medical devices distributed by FH ORTHO SAS for shoulder arthroplasty and traumatology, used in accordance with their approved labelling, in one of the centres participating in the Observatory (retrospectively or prospectively)\n2. Patient is at least 18 years of age\n3. Patient agreeing to participate after having been informed orally and in writing (with written consent if required locally) In some countries, such as France, the patient will have to be socially insured to be included in the study.\n\nExclusion criteria:\n\n1\\. Patient unable to participate in the study and\u002For complete the questionnaires 2. Refusal of patient participation\n\n\\-",{"count":103,"type":21},500,"OBSERVATIONAL","This study is a real-life observatory designed to collect long-term clinical data on patients who have undergone shoulder joint replacement or repair following shoulder trauma.\n\nIn this type of intervention, one or more medical devices distributed by FH ORTHO SAS may be used by surgeons.\n\nThis study meets the requirement for post-market clinical follow-up (PMCF) as defined in the European Medical Device Regulation (MDR 2017\u002F745).\n\nIt therefore involves collecting in real life, i.e. under the usual conditions of surgery and short and long-term patient follow-up, minimal clinical data that will make it possible to document the continued benefit\u002Frisk of the medical devices concerned.\n\nThis study is designed as a permanent long-term observatory, of a non-interventional nature, with the objective of having long-term follow-up data (5 to 10 years depending on the devices concerned) for a maximum number of patients included.",[107,28],"Trauma","2024-07-15",{"date":110,"type":35},"2024-07-22",{"date":112,"type":35},"2022-09-08",{"date":114,"type":21},"2035-09-08",{"name":116,"class":117},"FH ORTHO","INDUSTRY",3]