[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-pain-chronic\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-pain-chronic":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,55],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100646656","intralesional-versus-perilesional-5-dextrose-injection-in-partial-rotator-cuff-tears-100646656",false,"NCT07688902","Intralesional Versus Perilesional 5% Dextrose Injection in Partial Rotator Cuff Tears","Comparison of Clinical and Ultrasonographic Outcomes of Intralesional and Perilesional 5% Dextrose Injection in Patients With Partial Rotator Cuff Tears: A Prospective Randomized Double-Blind Controlled Trial","Inclusion Criteria:\n\n* Diagnosis of partial rotator cuff tear by a specialist physician after appropriate clinical examination and imaging evaluation\n* Shoulder pain and functional limitation lasting for at least 3 months\n* Clinically confirmed shoulder impingement findings, defined as at least one positive test among Neer, Hawkins-Kennedy, or painful arc tests\n* Age between 18 and 75 years\n* Ability to comply with the study procedures and attend follow-up visits regularly\n* Willingness to participate in the study and provide written informed consent\n\nExclusion Criteria:\n\n* Advanced cognitive impairment or dementia preventing reliable completion of questionnaires\n* Refusal to participate in the study or inability to provide informed consent\n* Full-thickness rotator cuff tear\n* Major tendon pathology other than the supraspinatus tendon, such as full-thickness subscapularis tear or biceps tendon rupture\n* Advanced acromioclavicular joint osteoarthritis, marked impingement, or marked adhesive capsulitis\n* Advanced glenohumeral joint arthritis\n* Active infection, cellulitis, or dermatologic lesion at the injection site\n* Bleeding diathesis or anticoagulant use\n* Known allergy or intolerance to dextrose injection\n* Intra-articular shoulder injection, including steroid, platelet-rich plasma, or prolotherapy, within the last 3 months\n* Previous shoulder surgery\n* Uncontrolled diabetes mellitus, defined as HbA1c \\>8.5%, or severe endocrine or metabolic disorder\n* Immunosuppression or active infection\n* Rheumatologic shoulder involvement\n* Neurological disease affecting shoulder movements\n* Pregnancy\n* Active malignancy","ALL","18 Years","75 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","This prospective, randomized, double-blind controlled clinical trial aims to compare the clinical and ultrasonographic outcomes of intralesional and perilesional 5% dextrose injection in patients with partial rotator cuff tears. Eligible participants will be randomized into two parallel groups. Both groups will receive ultrasound-guided 5% dextrose injection to the supraspinatus enthesis. In addition, one group will receive intralesional 5% dextrose injection, while the other group will receive perilesional 5% dextrose injection using the peppering technique. Injections will be performed in three treatment sessions at 21-day intervals. All participants will receive a home-based exercise program after completion of the injection treatments. Clinical outcomes will be assessed at baseline, 9 weeks, and 12 weeks after treatment, and ultrasonographic outcomes will be assessed at baseline and 12 weeks.",[27,28,29,30],"Partial Rotator Cuff Tears","Rotator Cuff Tendinopathy","Shoulder Pain Chronic","Supraspinatus Tendon Tear",[32,33,34,35,36,37,38,39,40,41],"Dextrose injection","Prolotherapy","Intralesional injection","Perilesional injection","Partial rotator cuff tear","Supraspinatus tendon","Ultrasound-guided injection","Shoulder Pain and Disability Index","Numeric Rating Scale","Ultrasonography","RECRUITING","2026-06-30",{"date":45,"type":46},"2026-07-07","ACTUAL",{"date":48,"type":46},"2025-02-01",{"date":50,"type":21},"2026-10-01",{"name":52,"class":53},"Ankara City Hospital Bilkent","OTHER",1,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":4,"eligibilityCriteria":61,"healthyVolunteers":62,"sex":16,"minAge":17,"maxAge":63,"enrollmentInfo":64,"targetDuration":4,"studyType":22,"phases":66,"briefSummary":67,"conditions":68,"keywords":70,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":54},"100555240","effect-of-the-modified-sleeper-stretch-on-the-elasticity-of-the-posterior-and-posteroinferior-glenohumeral-capsule-100555240","NCT06509516","Effect of the Modified Sleeper-Stretch on the Elasticity of the Posterior and Posteroinferior Glenohumeral Capsule","Quasi-experimental Study Protocol to Measure the Effect of Modified Sleeper-Stretch on the Elasticity of the Posterior and Posteroinferior Glenohumeral Capsule by Means of Shear Wave Elastography in Adult Population","Inclusion Criteria:\n\n* Male or female with clinical history of nonspecific shoulder pain on a single shoulder, who had GIRD of 15º or more, asymptomatic for more than one month and less than one year.\n* Male or female with no history of shoulder pain.\n* Age between 18 and 59 years.\n\nExclusion Criteria:\n\n* Glenohumeral osteoarthritis.\n* Labrum lesion, Bankart or Hill-Sachs lesion.\n* Posterior instability of any of the shoulders.\n* Evidence of joint hypermobility as defined by a Beighton Scale score greater or equal to 6.\n* Rotator cuff tear.\n* Fracture or surgery in the cervical region or in any of the upper limbs, except shoulders, if less than a year has passed since the episode.\n* History of surgical intervention in any of the shoulders.\n* Tumor growth in the shoulder region.\n* Neuromuscular injuries with shoulder muscles motor involvement (myasthenia, spinal cord injury, spastic contracture, paresis).\n* Inflammatory diseases (rheumatoid arthritis, psoriatic arthritis) affecting the shoulder region in state of outbreak.\n* Metabolic or systemic diseases with potential to modify tissue elastic capacity.\n* Diseases or injuries with contraindication to mobilization or physical exercise of the shoulder region.\n* Inability to perform the stretch due to pain.",true,"59 Years",{"count":65,"type":21},64,[24],"The goal of this quasi-experimental study is to determine the effect of the self-administered Modified Sleeper-Stretch on the elasticity of the posterior and posteroinferior glenohumeral capsule in adult individuals of both genders who either have clinical history of non-specific shoulder pain in a single shoulder or have no history of shoulder pain at all, being the assessment made by means of shear wave elastography. The main hypothesis it aims to confirm is:\n\n• A soft tissue stretching program, using the Modified Sleeper-Stretch, aimed at general adult population with history of nonspecific shoulder pain that has occurred with glenohumeral internal rotation deficit improves the elasticity of the posterior and posteroinferior glenohumeral capsules, showing no significant effect on general adult population without history of shoulder pain.\n\nResearchers will compare the effect of the Modified Sleeper-Stretch in the elasticity of the posterior and posteroinferior glenohumeral capsule in individuals with history of shoulder pain applying the technique on the affected shoulder and comparing with the healthy shoulder. In healthy individuals the intervention will be made on a randomly assigned shoulder and the effect will be compared to the non-interventional shoulder. Finally, a comparison between groups will be made considering only the intervention shoulder to see if there are differences in the effect amongst healthy and affected individuals.\n\nParticipants will be asked to follow a self-administered Modified Sleeper-Stretch program consisting of the execution of the stretch three times, for thirty seconds each time, with thirty seconds between stretches, daily, for twenty-eight days.",[69,29],"Shoulder Pain",[71,72,73,74],"Modified Sleeper-Stretch","Shear Wave Elastography","Posterior Capsule","GIRD","NOT_YET_RECRUITING","2024-07-28",{"date":78,"type":46},"2024-07-30",{"date":80,"type":21},"2024-09",{"date":82,"type":21},"2025-11",{"name":84,"class":53},"University of Alcala"]