[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-adhesive-capsulitis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-adhesive-capsulitis":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,44,68,95,128],{"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":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100618840","transcatheter-arterial-embolization-using-nexsphere-f-for-chronic-shoulder-pain-refractory-to-conservative-treatment-100618840",false,"NCT07336849","Transcatheter Arterial Embolization Using Nexsphere-F for Chronic Shoulder Pain Refractory to Conservative Treatment","A Single-center, Prospective, Open Label Randomized Clinical Trial to Evaluate the Efficacy and Safety of Transcatheter Arterial Embolization Using 'Nexsphere-F' in Patients With Adhesive Capsulitis of the Shoulder Joint Refractory to Conservative Treatment.","TAE-FROST","Inclusion Criteria:\n\n* Patients who have voluntarily signed a written informed consent form after receiving an explanation of the purpose, methods, and potential effects of the clinical trial\n\n  * Patients aged between 19 and 85 years\n\n    * Patients with pain persisting for more than 3 months in the affected area and with a history of receiving physical therapy, analgesics\u002Fanti-inflammatory medications, or local injection treatments\n\n      * Patients with a measured shoulder joint range of motion (ROM) of less than 90 degrees ⑤ Patients who agree not to receive any conservative treatment other than those permitted in this clinical trial (physical therapy, medication \\[NSAIDs, opioid analgesics, acetaminophen\\], intra-articular injections such as hyaluronic acid)\n\n        * Patients who are willing to comply with the treatment and procedures of the clinical trial and participate in all follow-up evaluations through hospital visits or telephone surveys\n\nExclusion Criteria:\n\n* Patients with a history of surgery on the shoulder joint targeted for the clinical trial prior to screening\n\n  * Patients suspected of having a full-thickness rotator cuff tear\n\n    * Patients with bleeding disorders or coagulopathies (e.g., idiopathic thrombocytopenic purpura, hemophilia, disseminated intravascular coagulation)\n\n      * Patients with advanced atherosclerosis or vasospasm in the arm vessels, or those expected to have such conditions\n\n        * Patients with a known hypersensitivity to gelatin\n\n          ⑥ Patients with a known hypersensitivity to contrast media\n\n          ⑦ Patients who are pregnant or breastfeeding\n\n          ⑧ Patients with a localized infection at the pain site\n\n          ⑨ Patients deemed inappropriate for participation by the investigator due to ethical concerns or potential impact on the clinical trial results","ALL","19 Years","85 Years",{"count":21,"type":22},44,"ESTIMATED","INTERVENTIONAL",[25],"NA","Evaluation of the efficacy and safety of transcatheter arterial embolization using 'Nexsphere-F' for pain relief in patients with adhesive capsulitis of the shoulder joint that does not respond to conservative treatment.\n\nThis study aims to investigate the efficacy and safety of transcatheter arterial embolization using embolic agents in patients with adhesive capsulitis of the shoulder joint. This is a single-center, prospective, open-label, randomized clinical trial.",[28,29,30],"Adhesive Capsulitis of the Shoulder","Frozen Shoulder","Shoulder Adhesive Capsulitis","RECRUITING","2026-05-18",{"date":34,"type":35},"2026-05-19","ACTUAL",{"date":37,"type":35},"2025-09-18",{"date":39,"type":22},"2027-08-31",{"name":41,"class":42},"Chung-Ang University Hosptial, Chung-Ang University College of Medicine","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":17,"minAge":50,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":23,"phases":53,"briefSummary":54,"conditions":55,"keywords":56,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":43},"100610444","feasibility-usability-and-preliminary-efficacy-of-home-based-fes-fro-adhesive-capsulitis-100610444","NCT07227662","Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis","Inclusion Criteria:\n\n1. Age \\> 18 years\n2. Individuals diagnosed with shoulder adhesive capsulitis\n3. Shoulder pain, limited shoulder mobility for more than 4 weeks, normal shoulder x-ray findings, and normal neurological exam\n4. Can tolerate electrical stimulation\n\nExclusion Criteria:\n\n1. Presence of shoulder tumors or bone lesions\n2. History of shoulder fracture or subluxation\n3. History of shoulder surgery\n4. Severe osteoporosis,\n5. Rheumatic disease\n6. Radiating pain from cervical radiculopathy\n7. Participation in other clinical trial, and\u002For intraarticular steroid injections within 6 weeks","18 Years",{"count":52,"type":22},10,[25],"The purpose of this study is to investigate the feasibility, usability and preliminary efficacy of a home-based Functional Electrical Stimulation(FES) in individuals with shoulder adhesive capsulitis. The main question it aims to answer is if combining home-based FES to usual therapy at the clinic will improve pain and improve function of the impaired shoulder.",[30],[57,58,30],"Functional Electrical Stimulation","Home-based","NOT_YET_RECRUITING","2026-05-15",{"date":34,"type":35},{"date":63,"type":22},"2026-06-01",{"date":65,"type":22},"2026-12-01",{"name":67,"class":42},"University of Maryland, Baltimore",{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":4,"eligibilityCriteria":74,"healthyVolunteers":11,"sex":75,"minAge":50,"maxAge":4,"enrollmentInfo":76,"targetDuration":4,"studyType":78,"phases":4,"briefSummary":79,"conditions":80,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":43},"100611136","deep-learning-for-musculoskeletal-complications-in-breast-cancer-100611136","NCT07236658","Deep Learning for Musculoskeletal Complications in Breast Cancer","AI-Powered Deep Learning Models for Prospective Prediction of Musculoskeletal Complications After Breast Cancer Surgery: Focus on Lymphedema, Axillary Web Syndrome, Neuropathy, and Pain","Inclusion Criteria:\n\nFemale sex Age ≥18 years Scheduled for surgery due to unilateral breast cancer\n\nExclusion Criteria:\n\nInability to comply with follow-up visits Bilateral breast cancer Male breast cancer Children (\\\u003C18 years) Pregnant women Postpartum women Breastfeeding women Individuals in intensive care Impaired consciousness Legally incapacitated individuals","FEMALE",{"count":77,"type":22},133,"OBSERVATIONAL","Survival after breast cancer has increased due to early diagnosis and advances in treatment methods. Musculoskeletal problems related to cancer and its treatment constitute a significant part of the daily practice of physiatrists and rehabilitation specialists involved in oncological rehabilitation.\n\nLymphedema can occur at any stage of a patient's life following breast cancer. Patients with breast cancer-related lymphedema require lifelong treatment, and as the stage of lymphedema progresses, response to therapy decreases. Advanced stages of lymphedema negatively affect functional status, and patients experience difficulties in performing activities of daily living.\n\nAxillary web syndrome (AWS) is characterized by a taut cord extending from the axilla to the volar surface of the wrist, typically appearing within the first 8 weeks postoperatively. AWS can complicate the administration of radiotherapy. Shoulder dysfunction may occur independently or in association with AWS. In particular, scapular dyskinesis developing after mastectomy can lead to secondary shoulder conditions such as rotator cuff syndrome or adhesive capsulitis, which are commonly observed in these patients.\n\nPeripheral neuropathy is frequently seen in patients receiving chemotherapy, adversely affecting daily life and sometimes preventing continuation of treatment. Other complications related to chemotherapy and radiotherapy include cardiotoxicity, pulmonary toxicity, fatigue, osteoporosis, and cognitive impairment.\n\nThere are also specific painful syndromes that may occur after breast cancer, including post-mastectomy pain syndrome, phantom breast pain, and musculoskeletal symptoms associated with aromatase inhibitors. All these conditions can significantly impair daily functioning and even hinder continuation of cancer treatment. Therefore, predicting these complications and implementing or developing preventive interventions is crucial.\n\nIf it is possible to predict the early development of lymphedema, axillary web syndrome, peripheral neuropathy, and painful syndromes after breast cancer, early intervention may prevent progression. This study is designed to develop and validate a predictive model using deep learning methods to determine the risk of these complications in patients undergoing breast cancer surgery. Among deep learning architectures, ResNet50, AlexNet, GoogleNet, and UNet, which have been widely used in recent studies, are planned to be implemented.\n\nAdditionally, based on the results of this study, a risk calculation program will be developed, allowing clinicians to input baseline patient data and calculate the individual patient's risk for each complication prior to treatment. No specific risk is expected in the study.",[81,82,83,30,84],"Postmastectomy Lymphedema Syndrome","Breast Cancer Surgery Pain","Osteoporosis Secondary","Axillary Web Syndrome","2026-03-30",{"date":87,"type":35},"2026-03-31",{"date":89,"type":35},"2025-07-01",{"date":91,"type":22},"2027-01-01",{"name":93,"class":94},"Ankara Etlik City Hospital","OTHER_GOV",{"id":96,"slug":97,"hasResults":11,"nctId":98,"briefTitle":99,"officialTitle":100,"acronym":4,"eligibilityCriteria":101,"healthyVolunteers":102,"sex":17,"minAge":50,"maxAge":4,"enrollmentInfo":103,"targetDuration":4,"studyType":23,"phases":105,"briefSummary":106,"conditions":107,"keywords":111,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":43},"100614097","hiit-for-inflammatory-driven-shoulder-pain-100614097","NCT07275164","HIIT for Inflammatory-driven Shoulder Pain.","Revolutionizing Musculoskeletal Shoulder Pain Management: High-intensity Interval Training as a Systemic Intervention. A Feasibility Study.","Inclusion Criteria:\n\nShoulder pain group\n\n* Shoulder pain \\> 3 months\n* Diagnosis of rotator cuff related shoulder pain or frozen shoulder\n* Understanding Dutch in speaking and writing.\n\nControl group\n\no Understanding Dutch in speaking and writing\n\nExclusion Criteria:\n\nShoulder pain group\n\n* \\\u003C18 years\n* Shoulder surgery or trauma in past year\n* Neurological, cancer, or neuromuscular disease\n* Osteoarthritis, cervical or AC joint pathology\n* Heavy physical exertion \\\u003C48h before testing\n\nControl group\n\n* \\\u003C18 years\n* recent or recurrent neck\u002Fshoulder pain\n* systemic or neurological disease\n* psychiatric disorders\n* pregnancy\u002Fbreastfeeding\n* pain medication \\\u003C48h before test",true,{"count":104,"type":22},30,[25],"This feasibility study investigates whether high-intensity interval training (HIIT) is feasible and acceptable for individuals with long-term shoulder pain where low-grade inflammation is suspected. Many patients do not recover fully with current local treatments, and systemic factors such as inflammation, and metabolic changes, additionally disturbances in the functioning of the nervous system often seem to play a role. HIIT is a time-efficient form of exercise that has been shown to improve inflammation and metabolic values and positively influence the balance of the nervous system. In this feasibility study, the investigators are enrolling 15 individuals with persistent shoulder pain (diagnosed with rotator cuff-related shoulder pain or frozen shoulder) with \\>3 months of symptoms, and 15 individuals without shoulder complaints. All participants will undergo measurements of inflammatory levels, glycosylated hemoglobin (HbA1c), blood pressure, body composition, pain sensitivity tests, and complete questionnaires about autonomic complaints and quality of life. Participants with shoulder pain will also perform one personalized HIIT session on a cycle ergometer. The investigators will assess whether participants accept a systemic intervention for their shoulder pain, if they are cooperative, and how they feel about the session; additionally, any side effects will be recorded. The aim is to determine whether HIIT is practically feasible and safe for this group and whether there are indications that systemic factors such as inflammation and nervous system function are associated with persistent shoulder pain. The outcome will determine whether follow-up research with a larger study is worthwhile.",[108,109,29,30,110],"Chronic Shoulder Pain","Rotator Cuff Related Shoulder Pain","Shoulder Pain",[112,113,114,115,116,117,118],"low-grade inflammation","chronic shoulder pain","autonomic dysfunction","metabolic syndrome","frozen shoulder","rotator cuff related shoulder pain","high intensity interval training","2026-02-10",{"date":121,"type":35},"2026-02-13",{"date":123,"type":35},"2025-12-10",{"date":125,"type":22},"2026-10",{"name":127,"class":42},"Universiteit Antwerpen",{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":11,"sex":17,"minAge":135,"maxAge":4,"enrollmentInfo":136,"targetDuration":4,"studyType":23,"phases":138,"briefSummary":139,"conditions":140,"keywords":141,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":148,"leadSponsor":150,"locationsCount":4},"100563613","scapular-mobilization-with-arm-movement-in-patients-with-adhesive-capsulitis-100563613","NCT06618443","Scapular Mobilization With Arm Movement in Patients With Adhesive Capsulitis.","Effect of Scapular Mobilization With Arm Movement on Shoulder Pain and Range of Motion and Disability in Older Adults With Adhesive Capsulitis.","Inclusion Criteria:\n\n* The existence of unilateral adhesive capsulitis (stage II) with incapability of the participant to raise the arm more than 100 degrees in the plane of the scapula\n\nExclusion Criteria:\n\n* The presence of any shoulder problem contraindicated for performing exercises to the shoulder joint, such as active inflammatory disease, cancer, active infection, recent subluxations or dislocations, fractures, and surgeries near the shoulder region.","65 Years",{"count":137,"type":22},50,[25],"50 patients with shoulder adhesive capsulitis were admitted. the patients will receive scapular mobilization (downward or upward mobilization) associated with arm movements. The percentage of improvement in shoulder ROM of flexion, abduction, and external rotation; and decrease in shoulder pain and disability index (SPADI).",[30],[142],"scapular mobilization; arm movement; pain; range of motion; disability; older adults; adhesive capsulitis","2024-09-30",{"date":145,"type":35},"2024-10-01",{"date":147,"type":22},"2024-10-15",{"date":149,"type":22},"2025-02-15",{"name":151,"class":42},"Beni-Suef University"]