[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"anterior-shoulder-dislocation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:anterior-shoulder-dislocation":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,47,85,109],{"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":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100424604","open-versus-arthroscopic-stabilization-of-shoulder-instability-with-subcritical-bone-loss-the-oasis-trial-100424604",false,"NCT04809064","Open Versus Arthroscopic Stabilization of Shoulder Instability With Subcritical Bone Loss: The OASIS Trial","OASIS","Inclusion Criteria:\n\n* Civilians and military personnel ages 17 to 50\n* Traumatic anterior shoulder dislocation\n* Associated subcritical bone loss between 10-20% less the glenoid width quantified by standard of care CT scan, MRI, or 3D-MRI scan\n* Had shoulder instability surgery using either 1) arthroscopic Bankart repair with remplissage of Hill-Sachs lesion; 2) open Bankart; or 3) Latarjet\n\nExclusion Criteria:\n\n* Chronic, non-traumatic multi-directional instability based on clinical exam\n* Concurrent shoulder injury in the involved shoulder (e.g., rotator cuff tears, motor nerve pathologies, osteoarthritis of a Samilson-Prieto grade \\>2)\n* Have a history of shoulder surgery in the involved shoulder (prior instability surgery that included any of the following and the planned procedure would be a repeat of the index procedure: 1) arthroscopic Bankart repair with a remplissage of Hill-Sachs lesion, 2) open Bankart, or 3) Latarjet \\[previous isolated arthroscopic Bankart repair only would not be an exclusion criterion\\], rotator cuff repair, intra-articular soft tissue surgery); rotator cuff repair, intra-articular soft tissue surgery)\n* Prior rotator cuff procedure on involved shoulder (including intra-articular soft tissue surgery\n* Humeral sided bone lesions (Hill-Sachs lesion) that is sufficiently large enough to render the lesion \"off-track\" even after a bony augmentation procedure would be performed\n* Neuromuscular, neurological and other movement control pathologies including seizures\n* Vascular injury associated with the shoulder trauma that compromise adequate\u002Fnormal healing or interferes with usual course of care\n* Traumatic brain injury or any condition that would preclude the ability to comply with post-operative guidelines\n* Cartilage lesion finding in the involved shoulder that would interfere with usual course of care\n* Known pregnancy at time of imagining and\u002For surgery based upon standard of care testing procedures\n* Any issue with the contralateral shoulder that would preclude participation in research procedures\n* Any condition in the opinion of the investigator\u002Fclinician that would preclude or limit full participation in study activities\n* Absence of a fixed address or no means of contact\n* Known inability to be available at all follow-up time points\n* Does not plan to return to pre-injury levels of work, sports or military duty","ALL","17 Years","50 Years",{"count":20,"type":21},450,"ESTIMATED","OBSERVATIONAL","This clinical trial will determine the outcome trajectories of common surgeries (arthroscopic Bankart repair with remplissage of a Hill-Sachs lesion, open Bankart, Latarjet) with post-operative rehabilitation and identification of prognostic factors among patients with acute or recurrent anterior shoulder instability with subcritical bone loss. The results of the study assist in optimizing time to return to military duty, work and sports, and patient-reported physical function for military personnel and civilians with traumatic anterior shoulder instability and 10-20% glenoid bone loss. This study will provide a critical clinical advancement of a previously unaddressed and common clinical scenario.",[25,26,27],"Shoulder Dislocation","Glenohumeral Dislocation","Anterior Shoulder Dislocation",[29,30,31,32,33],"Anterior Shoulder Instability","Glenoid Bone Loss","Stabilization Surgery","Return to Duty or Sport","Rehabilitation","RECRUITING","2026-06-04",{"date":37,"type":38},"2026-06-08","ACTUAL",{"date":40,"type":38},"2022-01-24",{"date":42,"type":21},"2027-09-30",{"name":44,"class":45},"University of Pittsburgh","OTHER",15,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":58,"studyType":22,"phases":4,"briefSummary":59,"conditions":60,"keywords":66,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":84},"100630343","shoulder-dislocation-assessment-of-lesions-trajectories-and-outcomes-salto-100630343","NCT07486440","Shoulder Dislocation: Assessment of Lesions, Trajectories and Outcomes (SALTO)","SALTO: Shoulder Dislocation: Assessment of Lesions, Trajectories and Outcomes. A Prospective Cohort of First-Time Anterior Shoulder Dislocations","SALTO","Inclusion Criteria\n\n* Age ≥16 years\n* Diagnosis of first-time traumatic anterior shoulder dislocation\n* Resident in the Oslo region who presents to Oslo Accident and Emergency Outpatient Clinic for treatment or follow-up within two weeks after initial injury\n* Ability to provide informed consent\n\nExclusion Criteria\n\n* Previous shoulder dislocation requiring reduction (Patients uncertain about prior dislocation are excluded)\n* Age \\\u003C 16 years\n* Chronic substance abuse affecting compliance\n* Inability to understand Norwegian or English\n* Adult not able to provide consent or severe medical or psychiatric condition precluding follow-up","16 Years",{"count":57,"type":21},180,"10 Years","The goal of this prospective observational cohort study is to provide epidemiological and prognostic data from a defined urban population and to improve understanding of risk factors and long-term outcomes following first-time anterior shoulder dislocation in patients aged 16 years and older presenting to the Oslo Accident and Emergency Outpatient Clinic.\n\nThe main questions the study aims to answer are:\n\n* What is the incidence of first-time anterior shoulder dislocations in the Oslo region?\n* What is the prevalence and extent of bipolar bone loss and soft tissue injuries measured by CT and MR after a first-time shoulder dislocation?\n* Does bone loss increase the risk of recurrent shoulder instability?\n* How do imaging findings and recurrence influence long-term shoulder function and quality of life?\n\nParticipants will:\n\n* Undergo standard clinical evaluation and conventional radiographs as part of routine care and asked to participate and followed longitudinally\n* Be offered additional CT and MRI imaging to assess glenoid and humeral bone loss and to evaluate soft tissue injuries.\n* Complete electronic questionnaires (WOSI, EQ-5D-5L, pain score, Rowe score, return to sport\u002Fwork) at 3 months, 1 year, 5 years, and 10 years.\n* Be invited to long-term follow-up, including radiographs at 10 years to evaluate signs of osteoarthritis.",[27,61,62,63,64,65],"Shoulder Dislocation Closed Traumatic","First Time Shoulder Dislocation","Shoulder Instability","Hill Sach Lesion","Bankart Lesion",[67,68,69,70,71,72,73],"First time shoulder dislocation","Shoulder instability","Primary shoulder dislocation","Recurrence","Bone loss","traumatic anterior shoulder dislocation","prospective","NOT_YET_RECRUITING","2026-03-18",{"date":77,"type":38},"2026-03-20",{"date":79,"type":21},"2026-04-15",{"date":81,"type":21},"2037-04",{"name":83,"class":45},"Oslo University Hospital",1,{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":4,"eligibilityCriteria":91,"healthyVolunteers":11,"sex":16,"minAge":92,"maxAge":4,"enrollmentInfo":93,"targetDuration":4,"studyType":95,"phases":96,"briefSummary":98,"conditions":99,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":84},"100502381","phase-4-methoxyflurane-or-virtual-reality-headset-vs-standard-analgesic-management-for-the-reduction-of-anterior-shoulder-dislocation-hypnolux-100502381","NCT05821517","METHOXYFLURANE or Virtual Reality Headset vs Standard Analgesic Management for the Reduction of Anterior Shoulder Dislocation (HYPNOLUX)","METHOXYFLURANE or Virtual Reality Headset vs Standard Analgesic Management for the Reduction of Anterior Shoulder Dislocation","Inclusion Criteria:\n\n* Pregnant and\u002For breastfeeding women and women of childbearing age who do not have effective contraception (hormonal, mechanical or surgical).\n* Patients with difficulties in understanding or using the devices studied.\n* Patients with a contraindication to the use of one of the studied devices.\n* Patients with a history of relevant shoulder surgery\n* Presence of other associated trauma,\n* Previous inclusion in the same study\n\nExclusion Criteria:\n\n* Withdrawal of voluntary informed consent from the patient\n* Violation of protocol\n* Presence of a fracture associated with the dislocation (excluding Malgaigne's notches)\n* Posterior, inferior or erecta dislocation\n* Presence of initial vascular and nerve complications\n* Any indication for surgical management","18 Years",{"count":94,"type":21},150,"INTERVENTIONAL",[97],"PHASE4","Anterior shoulder dislocation is a pathology frequently encountered in emergency medicine.\n\nThe success in reducing anterior shoulder dislocations depends on muscle relaxation, which is itself conditioned by the patient's pain and apprehension. However, there is no consensus on the optimal technique for reducing anterior shoulder dislocation or the analgesia associated with it.\n\nAnalgesia with METHOXYFLURANE showed a greater reduction in post-traumatic pain compared to standard analgesic treatment and faster action of METHOXYFLURANE. A retrospective study which has compared analgesia with METHOXYFLURANE and analgesic sedation with PROPOFOL found a shoulder reduction success rate of 80% and a reduction in the average length of stay in the emergency department.\n\nFinally, the use of virtual reality in pain management is emerging in our practices by allowing pre- and per-procedure hypno-sedation-analgesia. However, the use of virtual reality headsets has not been studied in the management of anterior shoulder dislocation.\n\nThe use of these two techniques could therefore limit the use of procedural sedation in the context of shoulder dislocation reduction.",[27],"2025-11-27",{"date":102,"type":38},"2025-12-04",{"date":104,"type":38},"2023-12-30",{"date":106,"type":21},"2027-03",{"name":108,"class":45},"Centre Hospitalier Universitaire de Nice",{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":4,"eligibilityCriteria":115,"healthyVolunteers":11,"sex":16,"minAge":92,"maxAge":116,"enrollmentInfo":117,"targetDuration":4,"studyType":95,"phases":119,"briefSummary":121,"conditions":122,"keywords":123,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":84},"100573920","apprehension-based-training-compared-with-standard-physical-therapy-for-military-personnel-following-anterior-shoulder-dislocation---a-randomized-clinical-trial-100573920","NCT06752551","Apprehension-based Training Compared With Standard Physical Therapy for Military Personnel Following Anterior Shoulder Dislocation - a Randomized Clinical Trial","Apprehension-based Training Compared With Standard Physical Therapy Among Military Personnel Following Anterior Shoulder Dislocation","Inclusion Criteria:\n\n* Age 18-39 years\n* Shoulder dislocation (primary or recurrent) documented by a medical practitioner (physician, military medic)\n* Positive anterior apprehension test\n* Gross shoulder muscle strength 3\u002F5 or greater\n\nExclusion Criteria:\n\n* Previous shoulder fracture, tendon tear, or shoulder surgery\n* Voluntary shoulder dislocation\n* Functional (Stanmore polar III) shoulder instability\n* Dislocation associated with a motor vehicle accident.\n* Diagnosis of rheumatoid arthritis, cancer (current), fibromyalgia, psychiatric disease)\n* Current pregnancy\n* Inability to attend at least one physical therapy session every 2 weeks.","39 Years",{"count":118,"type":21},85,[120],"NA","The goal of this clinical trial is to determine if a new rehabilitation protocol (apprehension-based training), leads to better recovery after shoulder dislocation among military personnel.\n\nParticipants will be randomly allocated to apprehension-based training or standard physical therapy. In apprehension-based training participants will train to control their shoulder under progressively more unstable conditions. Standard physical therapy will be provided based on the clinical judgment of the treating physical therapist The primary hypothesis is that participants undergoing apprehension-based training will experience a more complete recovery of function, better shoulder-related quality of life, and incur less recurrent dislocations.",[27],[124,125,68,126],"Randomized clinical trial","Anterior shoulder dislocation","Physical therapy","2025-06-02",{"date":129,"type":38},"2025-06-04",{"date":131,"type":38},"2025-02-05",{"date":133,"type":21},"2027-12-31",{"name":135,"class":45},"Alon Rabin"]