[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"arthroscopy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:arthroscopy":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,42,68,90],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100638867","comparison-of-two-general-anesthesia-maintenance-strategies-on-intraoperative-visibility-during-arthroscopic-rotator-cuff-surgery-a-randomized-trial-100638867",false,"NCT07628244","Comparison of Two General Anesthesia Maintenance Strategies on Intraoperative Visibility During Arthroscopic Rotator Cuff Surgery: A Randomized Trial","CLEAR-SHOULDER","Inclusion Criteria:\n\n1. Patient aged 18 or over\n2. Patient scheduled for elective rotator cuff repair arthroscopy (RCRA), performed in the \"beach-chair\" position under general anesthesia combined with an interscalene block (with or without standard associated procedures such as acromioplasty and\u002For tenotomy\u002Ftenodesis of the long biceps). Procedures for instability (Bankart\u002FLatarjet), fractures, capsulitis, simple lavage, or any arthroscopy not focused on rotator cuff repair (RCR) are not eligible.\n3. Patient with an ASA score of I to IV\n4. Patient affiliated to a social security scheme,\n5. Patient having given written consent following written and oral information.\n\nExclusion Criteria:\n\n1. Patients with a contraindication to any of the study agents, including known hypersensitivity or allergy to any of these agents or to any of their excipients.\n2. Patients with known coagulopathy (abnormal PT\u002FINR; platelets \\\u003C 100,000\u002FL) or\n3. Patients with active preoperative hemarthrosis or local infection.\n4. Non-elective (emergency) surgery or a procedure whose initial objective is not rotator cuff repair arthroscopy (RCRA). Note: Intraoperative conversion to open surgery is not an exclusion criterion; it will be considered an intraoperative event and managed in the analysis according to the intention-to-treat (ITT) principle, with a sensitivity analysis procedure described in the statistical plan.\n5. Uncooperative patient, inability to consent\n6. Pregnant women\n7. Patient protected by law under guardianship or curatorship, or unable to participate in a clinical study under article L. 1121-16 of the French Public Health Code.","ALL","18 Years",{"count":19,"type":20},110,"ESTIMATED","INTERVENTIONAL",[23],"NA","Shoulder arthroscopy is one of the most common orthopedic procedures, and the quality of the surgeon's view inside the joint is critical to its safety and success. Unlike limb surgery, no tourniquet can be applied to the shoulder, so surgical visibility depends almost entirely on how much bleeding occurs within the joint - which is itself influenced by the anesthetic drugs used to keep the patient asleep.\n\nTwo standard techniques exist for maintaining general anesthesia: inhaled anesthesia (sevoflurane) and total intravenous anesthesia (TIVA, using propofol). Evidence from other types of keyhole surgery (nasal, ear) suggests that propofol may produce better surgical visibility, possibly because sevoflurane causes slightly greater dilation of the smallest blood vessels in tissue, leading to more bleeding into the joint. However, in shoulder arthroscopy specifically, the data are scarce and contradictory.\n\nCLEAR-SHOULDER is a randomized, single-blind trial designed to determine whether propofol-based intravenous anesthesia provides superior intraoperative visibility compared to sevoflurane-based inhaled anesthesia during arthroscopic rotator cuff repair. Surgical visibility will be assessed from blinded video recordings of each procedure using the validated modified Fromme-Boezaart score. An exploratory artificial intelligence analysis of the arthroscopic videos will also be conducted.\n\nSecondary outcomes include operating time, irrigation fluid consumption, hemodynamic stability, vasopressor requirements, surgeon satisfaction, postoperative recovery, and environmental impact of each anesthetic strategy.",[26,27,28],"Rotator Cuff Injuries","Anesthesia, General","Arthroscopy","RECRUITING","2026-06-19",{"date":32,"type":33},"2026-06-24","ACTUAL",{"date":35,"type":33},"2026-06-18",{"date":37,"type":20},"2028-03-18",{"name":39,"class":40},"Centre Hospitalier Universitaire de Nice","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":49,"sex":16,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":54,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":41},"100489835","latarjet-vs-anatomic-glenoid-reconstruction-100489835","NCT05658289","Latarjet vs Anatomic Glenoid Reconstruction","Latarjet vs Anatomic Glenoid Reconstruction for Treatment of Anterior Shoulder Instability With Glenoid Bone Loss: a Prospective Multi-centre Randomized Trial","Inclusion Criteria:\n\n* Patients with one or more instances of anterior shoulder dislocation; pre-operative CT scan illustrating \\>20% bone loss.\n\nExclusion Criteria:\n\n* posterior shoulder instability; multidirectional shoulder instability; massive rotator cuff teats (MRI proven); history of substance abuse, patients unable to provide informed consent, patients refusing randomization.",true,"16 Years","40 Years",{"count":53,"type":20},68,[23],"Anterior shoulder dislocations occur when the humeral head translates anterior to the glenoid cause pain, stiffness, and glenoid bone loss. If left untreated, the risk of recurrence can be up to or greater than 90%. The only surgically modifiable factor to reduce the risk of recurrence is the glenoid bone loss (GBL), where surgeons have the ability to recreate the shape of the glenoid and reduce the risk of recurrent shoulder dislocations.\n\nEstablished boney procedures for shoulder instability include the Latarjet and free bone block procedures, such as the Anatomic Glenoid Reconstruction (AGR). The Latarjet is well known for its lower rate of recurrent instability, but raises concerns due to under-appreciated complications rates. The AGR is a newer surgical approach that has garnered attention for its low rate of recurrent instability and complication profile. Both treatments can reduce pain, increase function following surgery and reduce the risk of recurrent instability. However, these two established approaches have yet to be directly compared and studied on a larger scale.\n\nThe purpose of this randomized control trial is to compare clinical and radiographic outcomes pre- and post-operatively between the Latarjet to the AGR.",[57,58,28],"Shoulder Dislocation","Bone Loss","2024-08-20",{"date":61,"type":33},"2024-08-22",{"date":63,"type":33},"2023-04-24",{"date":65,"type":20},"2026-12",{"name":67,"class":40},"Nova Scotia Health Authority",{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":49,"sex":16,"minAge":17,"maxAge":74,"enrollmentInfo":75,"targetDuration":4,"studyType":21,"phases":77,"briefSummary":78,"conditions":79,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":41},"100553848","is-there-a-role-for-hip-arthroscopy-in-patients-with-femoral-head-fractures-100553848","NCT06491420","Is There a Role for Hip Arthroscopy in Patients With Femoral Head Fractures?","Inclusion Criteria:\n\n* Patients with pipkin 1 fractures\n\nExclusion Criteria:\n\n* any associated pelvic fractures\n* severe medical conditions that prevent the patient from undergoing surgery\n* delayed presentation after 2 weeks from initial fracture date","55 Years",{"count":76,"type":20},5,[23],"Femoral head fractures, often caused by high-energy trauma, pose significant challenges due to complications like avascular necrosis, post-traumatic osteoarthritis, and sciatic nerve damage. While traditionally treated with open reduction and internal fixation (ORIF) or total hip replacement (THR), hip arthroscopy has emerged as a minimally invasive alternative that reduces surgical trauma, offers direct fracture visualization and manipulation, and may result in shorter recovery times and fewer complications.",[80,28],"Femur Head Fracture","2024-07-01",{"date":83,"type":33},"2024-07-09",{"date":85,"type":33},"2022-01-01",{"date":87,"type":20},"2024-12-01",{"name":89,"class":40},"Kasr El Aini Hospital",{"id":91,"slug":92,"hasResults":11,"nctId":93,"briefTitle":94,"officialTitle":95,"acronym":4,"eligibilityCriteria":96,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":97,"enrollmentInfo":98,"targetDuration":4,"studyType":21,"phases":100,"briefSummary":101,"conditions":102,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":106,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":41},"100314255","clinical-and-radiographic-outcomes-after-amic-treatment-for-talus-osteochondral-lesion-trattamento-artroscopico-delle-lesioni-osteocondrali-dellastragalo-con-tecnica-amic-100314255","NCT03371121","Clinical and Radiographic Outcomes After AMIC Treatment for Talus Osteochondral Lesion Trattamento Artroscopico Delle Lesioni Osteocondrali Dell'Astragalo Con Tecnica AMIC","Valutazione Dell'Epidemiologia e Dei Risultati Radiografici e Clinici Nel Trattamento Artroscopico Delle Lesioni Osteocondrali Dell'Astragalo Con Tecnica AMIC","Inclusion Criteria:\n\n* Age over 18 years\n* males and females\n* patients underwent arthroscopic cartilage reconstruction surgery with AMIC technique for osteochondral lesions of the talus\n\nExclusion Criteria:\n\n* age \\\u003C18 years at the time of surgery\n* patients with previous surgery on the affected ankle","65 Years",{"count":99,"type":20},103,[23],"Aim of the study is to evaluate clinical and radiographic outcomes in patients undergone all-arthroscopic autologous matrix induced chondrogenesis for symptomatic osteochondral talar lesions",[103,104,28],"Talar Osteochondral Defect of Ankle","Pain","2017-12-07",{"date":107,"type":33},"2017-12-13",{"date":109,"type":33},"2016-04-26",{"date":111,"type":20},"2028-12",{"name":113,"class":40},"I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio"]