[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-tendinitis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-tendinitis":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,74],{"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":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100545060","phase-3-hyaluronic-acid-in-shoulder-tendinopathy-100545060",false,"NCT06376981","Hyaluronic Acid in Shoulder Tendinopathy","Benefit of a Subacromial Injection Combining Corticosteroid and Hyaluronic Acid Versus Corticosteroid Alone in Supraspinatus Tendinopathy","ACCTE","Inclusion Criteria:\n\n* Active patient aged between 18 and 65;\n* Patient suffering from pain compatible with supraspinatus tendinopathy for at least 2 months;\n* Patient with simple tendinopathy or partial tendon rupture;\n* Patient with tendinopathy confirmed by ultrasound or MRI;\n* Patient with an active pain visual analog scale ≥ 4 for more than 6 weeks;\n* Patient with an active pain visual analog scale ≥ 4 on the day of inclusion;\n* Patient failing medical treatment (rest, analgesics, NSAIDs, physiotherapy);\n* Patient able to follow the protocol and having given oral informed consent to take part in the research;\n* Patient affiliated to the social security system or entitled person;\n\nExclusion Criteria:\n\n* Patient suffering from a transfixing tendon rupture;\n* Patients suffering from post-traumatic tendon rupture;\n* Patients suffering from calcific tendinopathy (calcification \\> 5 mm);\n* Patients with associated glenohumeral osteoarthritis;\n* Patients with associated symptomatic acromioclavicular osteoarthritis;\n* Patients with shoulder pain for reasons other than tendinopathy (capsulitis, chronic inflammatory rheumatism, fibromyalgia, amyloidosis);\n* Patients who have had a subacromial infiltration in the previous 6 months;\n* Patients with a known allergy to one of the products including their excipients (methyl parahydroxybenzoate, propyl parahydroxybenzoate, benzyl alcohol);\n* Patients with a known allergy to lidocaine;\n* Patients with a local or generalised infection, or suspected infection;\n* Patients with severe coagulation disorders or taking anticoagulants;\n* Patients with severe and\u002For uncontrolled hypertension \\> 160\u002F100 mmHg;\n* Patients with unbalanced diabetes (last HbA1c \\> 8.5%);\n* Patients with a history of addiction to psychoactive substances;\n* Patient participating in another clinical research protocol with an impact on the research objectives;\n* Patient already randomised in the study;\n* Patient who is pregnant, parturient, breastfeeding or able to procreate without effective contraception\\* in the month prior to inclusion and up to 15 days after infiltration;\n* Patients under guardianship, curators or deprived of liberty;\n* Patient under a mandate for future protection activated ;\n* Patient under family guardianship ;\n* Patient under court protection ;","ALL","18 Years","65 Years",{"count":21,"type":22},132,"ESTIMATED","INTERVENTIONAL",[25],"PHASE3","Multicentric, randomised study to compare the effectiveness on activity pain at 3 months of corticosteroid injection associated with hyaluronic acid with corticosteroids injection alone in patients with tendinopathy of the supraspinatus with clinical reevaluation at one, three and six months.",[28],"Shoulder Tendinitis",[30,31,32],"Shoulder tendinitis","Hyaluronic acid","Corticosteroid injection","RECRUITING","2026-06-17",{"date":36,"type":37},"2026-06-22","ACTUAL",{"date":39,"type":37},"2024-09-19",{"date":41,"type":22},"2027-03-19",{"name":43,"class":44},"Centre Hospitalier Departemental Vendee","OTHER",2,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":23,"phases":56,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":45},"100634907","electroacupuncture-and-cupping-for-shoulder-tendinitis-100634907","NCT07545785","Electroacupuncture and Cupping for Shoulder Tendinitis","Effectiveness of Electroacupuncture Combined With Cupping Therapy in Patients With Shoulder Tendinitis and qi Stagnation and Blood Stasis Syndrome","Inclusion Criteria:\n\n* Patients between 18 and 70 years old.\n* Pain intensity score on the Visual Analogue Scale (VAS) between 4 and 7.\n* Diagnosis of rotator cuff and\u002For long head of the biceps tendonitis according to the guidelines issued by the Ministry of Health of Vietnam.\n* Mechanical pain that increases during movements such as abduction or raising the arm.\n* Presence of tender points at the long head of the biceps tendon or supraspinatus tendon .\n* Pain that increases during resisted contraction tests, such as the Jobe test or Palm-up test.\n* Absence of limitation in the passive range of motion of the shoulder.\n* Ultrasound findings showing a hypoechoic tendon or evidence of calcification.\n* Absence of motor weakness or paralysis.\n* Diagnosis of the TCM syndrome \"Qi Stagnation and Blood Stasis\"\n\nExclusion Criteria:\n\n* Patients who do not agree to participate in the study.\n* Diagnosis of pseudo-paralysis, acute calcific periarthritis, or frozen shoulder.\n* Shoulder pain caused by cervical nerve root lesions.\n* Shoulder pain originating from apical lung tumors, coronary artery disease, or myocardial infarction.\n* Specific joint lesions caused by infection, tuberculosis, or rheumatoid arthritis.\n* Bone pathologies including fractures, dislocations, or osteonecrosis of the humeral head.\n* Shoulder dysfunction resulting from stroke or hemiplegia.\n* Women who are pregnant.\n* Patients with mental illness.\n* Contraindications for vacuum cupping, such as acute skin inflammation, open wounds, or alcohol consumption.\n* Contraindications for electroacupuncture, including cardiac pacemakers, heart failure, or local skin ulcers.\n* Current participation in another intervention study.\n* Use of painkillers, muscle relaxants, or within the last week.\n* Use of anticoagulants or a history of hemophilia.","70 Years",{"count":55,"type":22},54,[57],"NA","This study aims to evaluate the effectiveness of electroacupuncture combined with vacuum cupping therapy in treating simple periarthritis of the shoulder associated with the traditional medicine syndrome of Qi stagnation and blood stasis. Shoulder periarthritis is a common condition that causes pain, stiffness, and limited movement of the shoulder due to injury or inflammation of the muscles, tendons, ligaments, and surrounding soft tissues. It can interfere with daily activities such as dressing, lifting objects, sleeping, and working.\n\nElectroacupuncture is commonly used to relieve shoulder pain and improve shoulder function. Vacuum cupping therapy is another non-drug treatment that may help improve blood circulation, reduce muscle tightness, decrease pain, and improve mobility. However, there is currently limited evidence about whether combining electroacupuncture with vacuum cupping provides better results than electroacupuncture alone in patients with shoulder periarthritis and Qi stagnation-blood stasis syndrome. This study is being conducted to determine whether the combined treatment is more effective and safe.\n\nA total of 54 participants with simple shoulder periarthritis and Qi stagnation-blood stasis syndrome will be enrolled in the study. Participants will be randomly assigned to one of two groups:\n\nGroup 1: treatment with electroacupuncture alone. Group 2: treatment with electroacupuncture combined with vacuum cupping therapy.\n\nAll participants will also receive advice on shoulder exercises, posture, and daily activities to support recovery. Treatments will be performed by licensed traditional medicine practitioners.\n\nEach participant will take part in the study for two weeks. Assessments will be performed before treatment, after one week, and after two weeks. The study will evaluate:\n\nPain intensity using the Visual Analogue Scale (VAS). Shoulder pain and disability using the Shoulder Pain and Disability Index (SPADI).\n\nShoulder range of motion using the McGill-McRomi Range of Motion Index. Any side effects or unwanted events related to treatment. Possible benefits of participating in this study include reduced shoulder pain, improved movement and daily function, and close monitoring by health care professionals. Participants may also benefit from receiving non-drug therapies at no cost during the study period. The findings of this research may help improve future treatment options for patients with shoulder pain.\n\nPossible risks of electroacupuncture include mild pain at the needle site, minor bleeding, bruising, dizziness, or fainting. Possible risks of vacuum cupping include temporary discomfort, skin redness, bruising, or mild pain in the treated area. These side effects are usually mild and temporary. If any unexpected problem occurs, participants will receive prompt medical attention.\n\nParticipation in this study is completely voluntary. Participants may refuse to join or may withdraw from the study at any time without affecting their usual medical care. All personal information collected during the study will remain confidential and will only be used for research purposes.",[60,28],"Shoulder Tendinopathy",[62,63,64,28],"shoulder tendinopathy","Rotator cuff tendinitis","Long head of the biceps tendonitis","2026-04-16",{"date":67,"type":37},"2026-04-22",{"date":69,"type":37},"2026-03-01",{"date":71,"type":22},"2026-11-15",{"name":73,"class":44},"University of Medicine and Pharmacy at Ho Chi Minh City",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":53,"enrollmentInfo":81,"targetDuration":83,"studyType":84,"phases":4,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":99},"100545632","subacromial-impingement-syndrome-functional-tests-correlation-with-ultrasound-parameters-100545632","NCT06384430","Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters","Subacromial Impingement Syndrome: The Relationship Between Shoulder Functional Tests and Ultrasound Parameters","Inclusion Criteria:\n\n1. Being between 18-70 years old\n2. Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)\n\nExclusion Criteria:\n\n1. Under 18, over 70 years of age\n2. Those diagnosed with rheumatologic diseases\n3. Those with symptomatic shoulder osteoarthritis\n4. Those with shoulder instability\n5. Shoulder pain in active, passive cervical spine movements\n6. Previous shoulder surgery\n7. Findings of adhesive capsulitis (\\>50% restriction of passive range of motion in 2 planes or detection of a full-thickness rotator cuff tear on ultrasound)\n8. Physiotherapy or intra-articular injection in the last 3 months\n9. Diagnosis of type 2 diabetes or hypothyroidism",{"count":82,"type":22},70,"1 Day","OBSERVATIONAL","In this study, among the patients who applied to the Physical Medicine and Rehabilitation outpatient clinic of Muğla Training and Research Hospital and were diagnosed with subacromial impingement by anamnesis and clinical tests, inclusion criteria) and exclusion criteria will be included in the study. Demographic data of the patients will then be recorded. DASH (Disabilities of the Arm, Shoulder and Hand) and Constant Murley scores will be calculated. 4 years of musculoskeletal ultrasound experience will be recorded by a radiologist using ultrasound (Siemens® V8, LA2-14A probe) in modified Crass position (positioning with the palm of the examined side on the posterior iliac wing) by measuring subacromial bursa thickness, supraspinatus tendon thickness, acromiohumeral distance, supraspinatus tendon thickness\u002Facromiohumeral distance ratio. Demographic data of the patients will then be recorded. DASH (Disabilities of the Arm, Shoulder and Hand) and Constant Murley scores will be calculated.",[87,28,88,89],"Subacromial Impingement Syndrome","Shoulder Bursitis","Shoulder Pain","2024-09-23",{"date":92,"type":37},"2024-09-25",{"date":94,"type":37},"2024-04-01",{"date":96,"type":22},"2024-10-31",{"name":98,"class":44},"Muğla Sıtkı Koçman University",1]