[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Xiros Ltd\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":67},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"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":4,"briefSummary":21,"conditions":22,"keywords":27,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100508867","post-market-clinical-follow-up-pmcf-study-of-the-pitch-patch-for-the-augmentation-or-reinforcement-of-the-rotator-cuff-100508867",false,"NCT05906004","Post-Market Clinical Follow-up (PMCF) Study of the Pitch-Patch for the Augmentation or Reinforcement of the Rotator Cuff","Inclusion Criteria:\n\n* Patient has been treated using a Pitch-Patch device for augmentation or reinforcement of the rotator cuff 2-2.5years prior to enrolment.\n* Patient has a baseline Constant Murley Score (CMS), assessed within 30 days prior to implantation of the device.\n* Patient must be 16 years old or above.\n* Patient is willing to participate in the study, and having been informed of the nature of the study, has provided written informed consent as approved by the Ethics Committee (EC).\n\nExclusion Criteria:\n\n\\- The Pitch-Patch has been used outside its intended use.","ALL","16 Years",{"count":18,"type":19},37,"ESTIMATED","OBSERVATIONAL","This is a clinical investigation study. It will verify the long-term safety and performance of the Pitch-Patch when implanted to reinforce partially repairable rotator cuff tears and used as described by the manufacturer's instructions.\n\nThe medical device in this study is already on the market and is manufactured by Xiros Ltd.\n\nThe Pitch-Patch is a single-use polyester prosthesis available in two sizes (30x20mm and 35x25mm). It is reinforced around the perimeter and around each eyelet to provide strength and stability to the device and repair.\n\nThe study will collect data on patients who meet the entry criteria and have received the device.\n\nThis is a single-armed study, meaning all patients will have a Pitch-Patch. The total length of the study is expected to be 3 years.\n\nA minimum of 37 patients will be enrolled into the study. Patients will be enrolled at a study specific follow up visit 2-2.5 years after implant, and data for baseline, procedure, and other time points prior to 2 years (3month, 6month, and 1 year post surgery) will be collected retrospectively from medical records if available.",[23,24,25,26],"Rotator Cuff Tear","Rotator Cuff Tears","Rotator Cuff Tears of the Shoulder","Rotator Cuff Injuries",[28,29,30,31,32],"Rotator Cuff Reinforcement","Rotator Cuff Repair","Pitch-Patch","Xiros","Rotator Cuff Augmentation","RECRUITING","2026-05-12",{"date":36,"type":37},"2026-05-15","ACTUAL",{"date":39,"type":19},"2026-05",{"date":41,"type":19},"2029-12",{"name":43,"class":44},"Xiros Ltd","INDUSTRY",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":66},"100469776","post-market-clinical-follow-up-pmcf-study-of-the-infinity-lock-button-system-for-acromioclavicular-joint-stabilisation-100469776","NCT05397210","Post-market Clinical Follow-up (PMCF) Study of the Infinity-Lock Button System for Acromioclavicular Joint Stabilisation","Post-market Clinical Follow-up (PMCF) Study of the Infinity-Lock™ Button System for Acromioclavicular Joint Stabilisation","Inclusion Criteria:\n\n* Patient must be 16 years old or above.\n\n  * Patient is diagnosed with acute or chronic Grade Ill-VI ACJ dislocation.\n  * Patient is willing to participate in the study and have been informed of the nature of the study, agree to its follow-up and have provided written informed consent as approved by the Research Ethics Committee (REC).\n\nExclusion criteria.\n\n* Known hypersensitivity to implant materials. If the patient is suspected of having any foreign body sensitivity, appropriate tests should be made prior to implantation.\n* Infections or any other structural or pathological condition of the bone or soft tissue (such as hyperlaxity) that would be expected to impair healing or secure fixation.\n* Patients unable or unwilling to restrict activities to prescribed levels or follow a rehabilitation programme during the healing period.\n* Skeletally immature patients are not suited as the Infinity-Lock™ Button System will not elongate with growth. The use of this medical device and placement of hardware or implants must not bridge, disturb or disrupt the growth plate.\n* Any other conditions or factors which in the opinion of the Investigator may interfere with study conduct.",{"count":54,"type":19},58,"This is a Post-market Clinical Follow-up Study. It will verify the long-term safety and performance of the Infinity-Lock Button System (ILBS) when used for acute and chronic dislocations of the Acromioclavicular Joint and used as described by the manufacturer's instructions.",[57],"Acromioclavicular; Dislocation","2026-01-26",{"date":60,"type":37},"2026-01-27",{"date":62,"type":37},"2022-09-26",{"date":64,"type":19},"2030-01",{"name":43,"class":44},4,""]