[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-dislocation-or-subluxation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-dislocation-or-subluxation":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,51,79,106],{"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":23,"studyType":24,"phases":4,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100631464","clinical-outcomes-of-arthroscopic-surgeries-for-shoulder-and-knee-sports-injuries-100631464",false,"NCT07501013","Clinical Outcomes of Arthroscopic Surgeries for Shoulder and Knee Sports Injuries","Clinical Outcomes and Associated Factors Following Arthroscopic Surgeries for Shoulder and Knee Sports Injuries: A Prospective Cohort Study","SK-COHORT","Inclusion Criteria:\n\n* Age \\>= 8 years.\n* No gender restrictions.\n* Definitive diagnosis of shoulder or knee sports injuries or related joint conditions.\n* Scheduled to undergo elective, standard-of-care surgery at the study center (procedures include but are not limited to: arthroscopic meniscus repair\u002Fmeniscectomy, cartilage repair, cruciate ligament reconstruction, high tibial osteotomy \\[HTO\\], unicompartmental knee arthroplasty \\[UKA\\], arthroscopic rotator cuff repair, shoulder stabilization, and shoulder arthroplasty).\n* Clear consciousness, with the ability to read, understand, and communicate.\n* Willing and able to comply with postoperative follow-up requirements.\n* Voluntarily signed the written informed consent form.\n\nExclusion Criteria:\n\n* Patients requiring emergency surgery due to acute, severe trauma (e.g., open fractures, polytrauma).\n* Coexisting severe neurological or psychiatric diseases, or cognitive impairment that prevents understanding of the informed consent or cooperation with follow-up.\n* Patients in an involuntary state (e.g., under coercion).\n* Refusal to sign the informed consent form or refusal to participate in the study.\n* Currently participating in other interventional clinical trials that may confound or affect the clinical outcomes of this study.","ALL","8 Years","80 Years",{"count":21,"type":22},500,"ESTIMATED","2 Years","OBSERVATIONAL","This observational study aims to evaluate the long-term recovery and clinical outcomes of patients undergoing minimally invasive (arthroscopic) surgeries for sports-related shoulder and knee injuries.\n\nSports injuries, such as ligament tears, meniscus damage, and rotator cuff tears, are common and can significantly impact a person's daily life and ability to return to sports. While surgery is an effective treatment, the recovery process and final outcomes can vary greatly from person to person.\n\nResearchers will follow patients who are already scheduled for routine shoulder or knee surgery at the study center. By collecting detailed information about the patient's initial injury, the specific surgical techniques used by the doctor, and the patient's recovery progress over two years, the study hopes to identify which factors lead to the best healing and functional outcomes.\n\nParticipants will be asked to complete standard questionnaires about their joint function and pain levels before their surgery, and again at 6 months, 1 year, and 2 years after surgery. The study is strictly observational; it will not change the standard medical care, surgical plan, or rehabilitation routine the patients receive.",[27,28,29,30,31,32],"Athletic Injuries (C26.857.500.124)","Rotator Cuff Injuries","Tibial Meniscus Injuries","Shoulder Dislocation or Subluxation","Anterior Cruciate Ligament Injuries","Posterior Cruciate Ligament Tear",[34,35,36,37,38],"Arthroscopy","Sports Medicine","Patient Reported Outcome Measures","Prospective Cohort","Clinical Outcomes","RECRUITING","2026-04-07",{"date":42,"type":43},"2026-04-13","ACTUAL",{"date":40,"type":43},{"date":46,"type":22},"2046-04-07",{"name":48,"class":49},"Second Affiliated Hospital, School of Medicine, Zhejiang University","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":17,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":63,"phases":64,"briefSummary":66,"conditions":67,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":78},"100601802","validation-of-an-upper-extremity-physical-performance-test-battery-in-patients-after-shoulder-dislocation-100601802","NCT07115225","Validation of an Upper Extremity Physical Performance Test Battery in Patients After Shoulder Dislocation","Predictive Validity of an Upper Extremity Physical Performance Test Battery in Patients After Shoulder Dislocation: a Prospective Study","VAL_PPT_P","Inclusion Criteria:\n\n* Practising sports with moderate to high demand on the shoulder (based on Degree of Shoulder Involvement in Sport (DOSIS) scale), minimal weekly 3 hours\n* Shoulder instability event (anterior direction)\n* Healthy contralateral shoulder\n* Completion of the postoperative rehabilitation protocol\n\nExclusion Criteria:\n\n* Other upper limb pathologies\u002F associated injuries: e.g. posterior instability, or rotator cuff tear,...\n* Being pregnant\n* No intention to return to pre-injury sport","16 Years","55 Years",{"count":62,"type":22},129,"INTERVENTIONAL",[65],"NA","The goal of this exploratory prospective study is to determine if an upper extremity test battery, comprised of physical performance tests, analytical tests and patient-reported outcome measures, can predict successful return to sports and quality of life in athletes (age 16-55) after shoulder dislocation.\n\nThe main research questions are:\n\n* Can an Upper Extremity Physical Performance Test Battery predict successful return to sports (= return to pre-injury sports level) in athletes after shoulder stabilization procedure\n* Can an Upper Extremity Physical Performance Test Battery predict the quality of life in athletes after shoulder stabilization procedure\n\nParticipants will:\n\n* Fill out questionnaires pre-operatively\n* Fill out the SIRSI questionnaire throughout the rehabilitation\n* Undergo a testing battery in the return to sport phase, including physical performance tests, analytical tests and patient-reported outcome measures\n* Fill out questionnaires every 3 months after return to sports, up to 1 year.",[68,30],"Return to Sport","2025-08-04",{"date":71,"type":43},"2025-08-11",{"date":73,"type":43},"2025-07-03",{"date":75,"type":22},"2029-01-01",{"name":77,"class":49},"University Ghent",2,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":59,"maxAge":87,"enrollmentInfo":88,"targetDuration":4,"studyType":63,"phases":90,"briefSummary":91,"conditions":92,"keywords":93,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":50},"100536193","rotofunc---non-traumatic-shoulder-instability-and-total-rotator-cuff-function-100536193","NCT06261645","Rotofunc - Non-traumatic Shoulder Instability and Total Rotator Cuff Function","ROTOFUNC - a Randomized and Controlled Study to Evaluate the Effect of a Novel Assessment and Treatment Strategy for Patients With Non-traumatic Shoulder Instability","ROTOFUNC","Inclusion Criteria:\n\n* young adults, non traumatic as well as non-controllable, positional, functional shoulder instability according to Moroder et al. demonstrating a lack of ≥ 20%, active, dynamic control compared with the total passive range of motion in shoulder rotation with or without previous shoulder stabilizing surgery\n* Understanding the Swedish language well, in speaking, in reading and writing.\n\nExclusion Criteria:\n\n* Other significant shoulder pathologies, patients diagnosed with severe systemic connective tissue, congenital anatomic abnormalities, or psychiatric diagnoses according to previous medical records\n* \\\u003C60% adherence to assigned exercises","35 Years",{"count":89,"type":22},100,[65],"The goal of this clinical trial is to test the effect of a novel assessment and treatment strategy for young adults with severely disabling non-traumatic shoulder instability. The main question it aims to answer is if this treatment will substantially change the patients shoulder function to a more stable and controllable state and thereby give a higher quality of life. Participants failure in active shoulder muscle function will be assessed and exercises will be selected individually. Patients will be asked to perform the exercises twice per day. At clinical visits to a specialized physiotherapist the exercises will be upgraded to restore full dynamic stability throughout shoulder movement range. The active treatment period will be 4 months. Researchers will compare two groups. One group will start directly after a baseline assessment is fulfilled. The other group will receive the treatment with a delay of 4 months to evaluate if the selected exercises can substantially change the shoulder stability compared to no treatment, the natural course of the condition.",[30],[94,95,96],"physiotherapy","muscle control","non-surgical","2024-03-06",{"date":99,"type":43},"2024-03-08",{"date":101,"type":43},"2023-05-01",{"date":103,"type":22},"2026-12",{"name":105,"class":49},"Sahlgrenska University Hospital",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":112,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":17,"minAge":114,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":63,"phases":117,"briefSummary":118,"conditions":119,"keywords":4,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":4},"100528166","multifactorial-approach-training-for-anterior-shoulder-instability-in-patients-undergoing-arthroscopic-bankart-repair-100528166","NCT06157229","Multifactorial Approach Training for Anterior Shoulder Instability in Patients Undergoing Arthroscopic Bankart Repair","Multifactorial Approach Training for Anterior Shoulder Instability in Patients Undergoing Arthroscopic Bankart Repair, a Randomized Controlled Trial","MATASI","Inclusion Criteria:\n\n* Primary or recurrent traumatic anterior shoulder dislocation (MRI-confirmed labral tear)\n* Aged between 18-67 years\n* Planned arthroscopic Bankart repair (ABR) surgery\n* Understanding of spoken and written Dutch language\n* Written informed consent (according to the ICH-GCP guidelines)\n* Positive apprehension sign at physical examination\n\nExclusion Criteria:\n\n* Posterior or multidirectional shoulder instability\n* Presence of hyperlaxity of the upper extremity and absence of sulcus sign and \\>85 degrees of external rotation with the arm at the side at physical examination\n* Connective tissue disorders (e.g. Ehlers-Danlos)\n* Aged \\\u003C18 or \\>67 years\n* Assymetry in rotator cuff strength, bilateral component ((sub)luxations on contralateral side)\n* History of soft tissue repair or bone block procedure on one of both shoulders\n* Current or past anxiety disorders or use of anxiety supressing drugs (e.g. anti-psychotics)\n* Implantable cardioverter defibrillator (ICD) (unable to be included for functional MRI)\n* Neurological disorders or systemic disease\n* Loss of anteroinferior sclerotic contour of the glenoid on AP view of the shoulder\n* Hill-Sachs lesion visible on external rotation radiographs\n* Greater tubercle fracture","18 Years","67 Years",{"count":89,"type":22},[65],"This study will compare functional outcomes after an arthroscopic Bankart repair between patients that underwent conventional arthroscopic Bankart repair rehabilitation, following the American Society of Shoulder and Elbow Therapists guideline and patients that underwent 'multifactorial approach training', which focusses on decreasing kinesiophobia and fear of recurrent dislocations.\n\nThe study population comprises patients who will undergo Arthroscopic Bankart Repair (ABR) after a traumatic anterior shoulder dislocation at Spaarne Gasthuis Haarlem\u002FHoofddorp, OLVG Amsterdam, Amstelland Ziekenhuis Amstelveen, Gelre Ziekenhuizen, Medisch Spectrum Twente, or Flevoziekenhuis Almere.",[120,30,121,122],"Shoulder Instability","Fear of Movement","Kinesiophobia","NOT_YET_RECRUITING","2023-11-27",{"date":126,"type":43},"2023-12-05",{"date":128,"type":22},"2024-01-01",{"date":130,"type":22},"2027-06-01",{"name":132,"class":49},"Spaarne Gasthuis"]