[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100491286":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":26,"centralContacts":30,"locations":39,"responsibleParty":56,"collaborators":59,"id":63,"slug":64,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":69,"eligibilityCriteria":70,"healthyVolunteers":65,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":25,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":84,"overallStatus":42,"whyStopped":25,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":97},{"fullName":5,"class":6},"AUVA Traumazentrum Vienna Site UKH Meidling","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Zoledronic Acid","ACTIVE_COMPARATOR","zoledronic acid 5 mg (Aclasta®) administered as single intravenous infusion (100 ml): Verum",[13],"Drug: Intravenous Infusion of Aclasta®",{"label":15,"type":16,"description":17,"interventionNames":18},"physiological saline solution 0.9%","PLACEBO_COMPARATOR","Sodium chloride (physiological saline solution 0.9%) administered as single intravenous infusion (100 ml): Placebo",[13],[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","Intravenous Infusion of Aclasta®","Intravenous Infusion of Aclasta® (Verum) or physiological saline solution 0.9% (Placebo)",[9,15],null,[27],{"name":28,"affiliation":5,"role":29},"Jakob Schanda, DDr.","PRINCIPAL_INVESTIGATOR",[31,35],{"name":28,"role":32,"phone":33,"phoneExt":25,"email":34},"CONTACT","+435939345201","jakob.schanda@auva.at",{"name":36,"role":32,"phone":37,"phoneExt":25,"email":38},"Ortrun Neuper, MSc.","+436764543334","oneuper@trauma.lbg.ac.at",[40],{"facility":41,"status":42,"city":43,"state":25,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"Jakob Schanda","RECRUITING","Vienna","1120","Austria","AT",{"type":48,"coordinates":49},"Point",[50,51],16.37208,48.20849,{"lat":51,"lon":50},[54,55],{"name":28,"role":32,"phone":33,"phoneExt":25,"email":34},{"name":36,"role":32,"phone":37,"phoneExt":25,"email":38},{"type":29,"investigatorFullName":41,"investigatorTitle":57,"investigatorAffiliation":58,"oldNameTitle":25,"oldOrganization":25},"Principal Investigator","AUVA Trauma Center Meidling",[60],{"name":61,"class":62},"Ludwig Boltzmann Institute for Traumatology - The research center in cooperation with AUVA","OTHER_GOV","100491286","phase-2-influence-of-an-anti-osteoporotic-drug-on-healing-after-surgical-repair-of-chronic-rotator-cuff-lesions-of-the-shoulder-100491286",false,"NCT05677152","Influence of an Anti-osteoporotic Drug on Healing After Surgical Repair of Chronic Rotator Cuff Lesions of the Shoulder","Influence of Zoledronic Acid on Healing After Arthroscopic Repair of Chronic Rotator Cuff Lesions - A Prospective, Randomized, Placebo-controlled Phase II Trial","ZORRO","Inclusion Criteria\n\n* Age between 50 and 70 years\n* Magnetic resonance imaging verified rotator cuff tear (within 6 month prior to surgery)\n* Rupture size with a maximum diameter of 3 cm\n* Willingness to participate in the study\n* Willingness to participate in a unified physiotherapy with use of a shoulder abduction pad for four weeks postoperativel\n\nExclusion Criteria:\n\n* Patients younger than 50 or older than 70 years of age\n* Pregnancy\n* Known allergy to zoledronic acid or other components of the medicinal product\n* Previous fracture of the affected shoulder\n* Previous surgery of the affected shoulder\n* Previous or existing bacterial infection of the affected shoulder\n* Rupture of more than two tendons in the affected shoulder (massive rotator cuff tear)\n* Isolated subscapularis tendon tear\n* Presence of glenohumeral osteoarthritis (Hamada type 3 or higher)\n* Diabetes mellitus (fasting glucose ≥ 126 mg\u002Fdl, HbA1C ≥ ZORRO Version Draft1.0\u002F09.05.2022 Page 6 of 42 6.5%)\n* Malignant tumor disease\n* Pathological dental status\n* Known disease that interferes with bone metabolism\n* Concomitant diseases that do not permit general anesthesia\n* Previous therapy with anti-osteoporotic drugs (bisphosphonates, denosumab, teriparatide)\n* Epilepsy\n* Claustrophobia\n* Chronic alcohol abuse\n* Drug abuse","ALL","50 Years","70 Years",{"count":75,"type":76},80,"ESTIMATED","INTERVENTIONAL",[79],"PHASE2","This is a prospective, single-center, placebo-controlled, non-comparative, phase II study to evaluate the influence of an adjuvant, intravenous therapy with zoledronic acid (single dose) on healing after arthroscopic repair of chronic rotator cuff tears.\n\nThe study including its financial support was approved by the medical director of the General Accident Insurance Institution (AUVA) , Dr. Roland Frank.\n\nHypothesis to prove: Adjuvant intravenous therapy with zoledronic acid does improve tendon healing after arthroscopic reconstruction of chronic rotator cuff tears compared to a control group without adjuvant therapy with zoledronic acid.,",[82,83],"Orthopedics","Traumatology",[85,86,87],"zoledronic acid","chronic rotator cuff tears","arthroscopic repair","2024-03-14",{"date":90,"type":91},"2024-03-18","ACTUAL",{"date":93,"type":91},"2022-08-22",{"date":95,"type":76},"2030-12",{"name":5,"class":6},1]