[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"rotator-cuff-repairs\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:rotator-cuff-repairs":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,40,70,90],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100053460","phase-4-the-effect-of-multimodal-pain-regimen-on-use-of-narcotics-after-rotator-cuff-tear-repair-100053460",false,"NCT07076069","The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair","Inclusion Criteria:\n\n* Adults with rotator cuff tears who have failed conservative therapy and are now undergoing arthroscopic rotator cuff repair.\n\nExclusion Criteria:\n\n* Patients without capacity to consent for the study\n* Patients not able to have local nerve block\n* Patients who underwent previous shoulder surgery on the same side, kindling revision rotator cuff repair\n* Patients who are unable to record and verbalize their pain level due to altered mental status\n* Patients who are unable to tolerate any of the medications included in the multimodal pain regimen or standard pain regimen due to severe allergies or inability to consume medication\n* Patients with history of previously diagnosed alcohol or drug abuse, renal impairment, peptic ulcer disease, and gastrointestinal bleeding\n* Patients who are pregnant","ALL","18 Years",{"count":18,"type":19},130,"ESTIMATED","INTERVENTIONAL",[22],"PHASE4","The goal of this clinical trial is to understand which group of pain control medications work best in adults after rotator cuff surgery.",[25,26],"Rotator Cuff Repairs","Pain Management","RECRUITING","2026-07-10",{"date":30,"type":31},"2026-07-13","ACTUAL",{"date":33,"type":31},"2025-07-21",{"date":35,"type":19},"2028-06",{"name":37,"class":38},"Montefiore Medical Center","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":15,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":52,"phases":4,"briefSummary":53,"conditions":54,"keywords":55,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":4},"100623262","impact-of-rotator-cuff-repair-on-rehabilitation-outcome-100623262","NCT07394348","Impact of Rotator Cuff Repair on Rehabilitation Outcome","Impact of Biceps Tenotomy Versus Tenodesis on Rehabilitation Outcomes After Rotator Cuff Repair","Inclusion Criteria:\n\nThe participant's selection will be based on the following criteria:\n\n1. Both genders adults diagnosed with ≥ 1-cm full-thickness tears of rotator cuff.\n2. Age ranged from 50 to 70 years .\n3. LHB pathology is involved that will receive ARCR combined with biceps tenotomy or tenodesis.\n4. Arthroscopically confirmed LHB pathology.\n5. Functionality according to their physical level -\n\nExclusion Criteria:\n\nParticipants will be excluded if they have any of the following criteria:\n\n1. Massive irreparable tears.\n2. Inflammatory arthritis.\n3. Thyroid disease.\n4. Glenohumeral osteoarthritis.\n5. Severe cervical disorders or paralysis of the axillary nerve.\n6. Previous surgery of the affected shoulder.\n7. Revision surgeries for a rotator cuff tear.\n8. Complete LHBT rupture. -",true,"50 Years","70 Years",{"count":51,"type":19},50,"OBSERVATIONAL","This study will investigate the difference between BTT (biceps tenotomy ) versus BTD (biceps tenodesis)in patients undergoing rotator cuff repair on postoperative shoulder pain levels, shoulder function, HGS, forearm supination muscle strength, elbow flexion strength",[25],[56,57,58,59],"Biceps tenotomy","Biceps tenodesis","Rehabilitation outcomes","Hand grip strength","NOT_YET_RECRUITING","2026-02-03",{"date":63,"type":31},"2026-02-06",{"date":65,"type":19},"2026-02-01",{"date":67,"type":19},"2027-03",{"name":69,"class":38},"Cairo University",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":52,"phases":4,"briefSummary":79,"conditions":80,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":39},"100599127","pmcf-study-on-the-safety-performance-and-clinical-benefits-data-of-the-compositcp-100599127","NCT07080450","PMCF Study on the Safety, Performance and Clinical Benefits Data of the ComposiTCP","Post-market Clinical Follow-up Study to Collect Safety, Performance and Clinical Benefits of the ComposiTCP™ Suture Anchors Double Loaded With BroadBand Tape, Sliding","Inclusion Criteria:\n\n* Subject was treated with the ComposiTCP Suture Anchors Double Loaded with BroadBand Tape, Sliding for rotator cuff repair;\n* At least 18 years old and skeletally mature;\n* Willing and able to comply with the study procedures;\n* Subject is capable of understanding the doctor's explanations, following his instructions and is able to participate in the follow-up program;\n* Subject is able to read and understand the ICF and has voluntarily provided written informed consent or non-opposition.\n\nExclusion Criteria:\n\n* Subject is vulnerable (is unable to fully understand all aspects of the investigation that are relevant to the decision to participate, or who could be manipulated or unduly influenced as a result of a compromised position, expectation of benefits or fear of retaliatory response);\n* The subject is unwilling or unable to give consent or to comply with the follow-up program;\n* Subject meets any contraindications of the appropriate Instruction for Use;\n* Off-Label Use.",{"count":78,"type":19},43,"The study is a multicenter, retrospective and prospective, non-randomized, noncontrolled, and consecutive series post-market study. The purpose of this study is collect data confirming safety, performance and clinical benefits of the ComposiTCP Suture Anchors Double Loaded with BroadBand Tape, Sliding implants when used in rotator cuff repair.\n\nThe primary endpoint of this study is the assessment of performance by analyzing soft tissue to bone healing in the shoulder (rotator cuff). Healing will be assessed by the investigator using PROMs and clinical outcomes of the patient.\n\nThe clinical benefit will be assessed by functional outcomes measured using standard and well-established scoring systems (e.g. Oxford Shoulder Score and EQ-5D-5L) at 1 year post-operative.\n\nThe safety will be assessed by monitoring the incidence and frequency of device- and\u002For procedure-related adverse events.",[25],"2026-02-02",{"date":61,"type":31},{"date":84,"type":31},"2025-07-01",{"date":86,"type":19},"2026-08",{"name":88,"class":89},"Zimmer Biomet","INDUSTRY",{"id":91,"slug":4,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":20,"phases":93,"briefSummary":23,"conditions":94,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":99,"leadSponsor":101,"locationsCount":39},"100598790",{"count":18,"type":19},[22],[25,26],"2026-01-12",{"date":97,"type":31},"2026-01-13",{"date":33,"type":31},{"date":100,"type":19},"2026-06-01",{"name":37,"class":38}]