[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Christian Candrian\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":112},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,41,65,88],{"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":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100400472","a-study-to-verify-if-the-surgery-for-the-proximal-femur-fracture-can-be-improved-with-the-help-of-a-navigation-system-100400472",false,"NCT04494672","A Study to Verify if the Surgery for the Proximal Femur Fracture Can be Improved With the Help of a Navigation System","Improving Intramedullary Nailing of Proximal Femoral Fractures Through a Navigation Assisted Technique: a Double Blinded Randomized Control Trial","Inclusion Criteria:\n\n* Patients undergoing unilateral primary intramedullary nailing at the Ospedale Regionale di Lugano.\n* Patients aged 50-85 years old.\n* Patients with a BMI \\>18 and \\\u003C35.\n* Patients able to provide informed consent and follow all the study procedures as indicated by the protocol.\n* Radiological evidence of proximal fracture of the femur, AO classified as 31 A1.3, 31 A2.1, 31 A2.2, 31 A2.3, 31 A3.1, 31 A3.2, 31 A3.3.\n\nExclusion Criteria:\n\n* Other clinically significant concomitant disease states (e.g. renal failure, major hepatic dysfunction, life-threatening cardiovascular disease, etc..).\n* Known or suspected non-compliance, drug or alcohol abuse.\n* Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant.\n* Previous enrolment into the current study.\n* Enrolment of the investigator, his\u002Fher family members, employees and other dependent persons.","ALL","50 Years","85 Years",{"count":20,"type":21},96,"ESTIMATED","INTERVENTIONAL",[24],"NA","The ADAPT system is a software that calculate a virtual 3D reconstruction of the femoral head without additional radiation. It automatically detects the used implant and its position relative to the femoral head, helping the surgeon to achieve an optimal proximal screw positioning in the femoral head. The investigators want to verify if with the addition of the ADAPT system the investigators can improve screw placement and reduce surgery time and radiation exposure.",[27],"Femoral Fracture","RECRUITING","2026-03-03",{"date":31,"type":32},"2026-03-05","ACTUAL",{"date":34,"type":32},"2020-09-28",{"date":36,"type":21},"2026-08-01",{"name":38,"class":39},"Christian Candrian","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":48,"maxAge":18,"enrollmentInfo":49,"targetDuration":4,"studyType":22,"phases":51,"briefSummary":53,"conditions":54,"keywords":56,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":59,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":40},"100401451","phase-4-intravenous-dexamethasone-administration-in-patients-undergoing-total-shoulder-arthroplasty-100401451","NCT04507412","Intravenous Dexamethasone Administration in Patients Undergoing Total Shoulder Arthroplasty","Effect of Perioperative Intravenous Dexamethasone Administration in Patients Undergoing Total Shoulder Arthroplasty for Osteoarthritis, in Terms of Post-operative Pain, Function, Nausea, Hospitalization Length, and Risk of Complications","Inclusion Criteria:\n\n* Patients undergoing unilateral primary total anatomical or reverse shoulder arthroplasty (Total Shoulder Arthroplasty)\n* Patients with a BMI \\>18.5 and \\\u003C35\n* Patients able to provide informed consent and follow all the study procedures as indicated by the protocol\n* Informed Consent as documented by signature\n\nExclusion Criteria:\n\n* Contraindications to steroids\n* Revision and post-traumatic TSA\n* Active steroid or immunosuppressive therapy in the last 30 days before the operation\n* Pregnant or breast-feeding women\n* Presence of other clinically significant concomitant disease states (ASA IV)\n* Uncontrolled diabetes mellitus\n* Contraindications to Non-steroidal anti-inflammatory drugs\n* Chronic systemic diseases as immunodeficiency, autoimmune disease (Systemic Lupus Erythematosus), gout, rheumatic arthritis\n* Known or suspected non-compliance, drug or alcohol abuse\n* Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant.\n* Participation in another study with investigational drug within the 30 days preceding and during the present study\n* Previous enrolment into the current study\n* Enrolment of the investigator, his\u002Fher family members, employees and other dependent persons","58 Years",{"count":50,"type":21},74,[52],"PHASE4","The aim of the study is to evaluate if intravenous steroid supplementation can provide advantages over routine analgesia protocols in terms of post-operative symptoms (pain and nausea), length of hospital stay, shoulder range of motion, function and patient satisfaction",[55],"Arthroplasty, Replacement, Shoulder",[57,58],"Total Shoulder Arthroplasty","steroid",{"date":31,"type":32},{"date":61,"type":32},"2020-09-09",{"date":63,"type":21},"2032-08-31",{"name":38,"class":39},{"id":66,"slug":67,"hasResults":11,"nctId":68,"briefTitle":69,"officialTitle":70,"acronym":4,"eligibilityCriteria":71,"healthyVolunteers":11,"sex":16,"minAge":72,"maxAge":17,"enrollmentInfo":73,"targetDuration":4,"studyType":22,"phases":75,"briefSummary":76,"conditions":77,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":87},"100443380","this-is-a-study-to-verify-if-marrow-venting-procedure-can-improve-meniscal-suture-healing-100443380","NCT05053646","This is a Study to Verify if Marrow Venting Procedure Can Improve Meniscal Suture Healing","Biological Augmentation Of Meniscal Repair With Marrow Venting: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Arthroscopic confirmed suturable meniscal tears,\n* Monolateral meniscal tears,\n* 18-45 years,\n* BMI\\>18,5 and \\\u003C35 kg\u002Fm2,\n* Ability to give informed consent by signature.\n\nExclusion Criteria:\n\n* Bilateral meniscal tears requiring treatment,\n* Associated ligament lesions requiring treatment,\n* Associated cartilage lesions (Outerbridge \\> 2),\n* Knee axis deformities requiring correction\n* Generalized ligamentous laxity,\n* Radiographic knee ostheoarthritis,\n* Other reasons for knee pain,\n* Pregnant or lactating women,\n* Serious systemic diseases such as cardiac, hepatic or renal failure, rheumatic diseases, non-compensated diabetic, psychological illnesses, central or peripheral neurological diseases, and autoimmune diseases,\n* Enrolled in another ongoing clinical trial.","16 Years",{"count":74,"type":21},80,[24],"Meniscal suture represents the current surgical practice, and marrow venting is a low risk procedure. Bone venting may be able to improve the outcome of meniscal repair, allowing the patient a better recovery.",[78],"Meniscal Tear","2025-08-05",{"date":81,"type":32},"2025-08-06",{"date":83,"type":32},"2021-12-29",{"date":85,"type":21},"2030-10-01",{"name":38,"class":39},2,{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":4,"eligibilityCriteria":94,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":95,"targetDuration":4,"studyType":22,"phases":97,"briefSummary":98,"conditions":99,"keywords":101,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":106,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":40},"100395662","phase-4-a-study-to-compare-different-ways-of-steroid-administration-after-total-knee-implantation-100395662","NCT04432012","A Study to Compare Different Ways of Steroid Administration After Total Knee Implantation","Comparison of Perioperative Intravenous vs Periarticular Dexamethasone vs no Steroid Supplementation in Terms of Post-operative Pain, Function, Nausea, Hospitalization Length, and Risk of Complications in Patients Undergoing Primary Total Knee Arthroplasty for Knee Osteoarthritis - A Randomized Controlled Trial Clinical Study Protocol","Inclusion Criteria:\n\n* Patients undergoing unilateral primary TKA at the Ospedale Regionale di Lugano.\n* Patients with a BMI \\>18.5 and \\\u003C35.\n* Patients able to provide informed consent and follow all the study procedures as indicated by the protocol.\n* Informed Consent as documented by signature (Appendix Informed Consent Form).\n\nExclusion Criteria:\n\n* Contraindications to steroids.\n* Revision TKA.\n* Active steroid therapy.\n* Women who are pregnant or breast feeding.\n* Presence of other clinically significant concomitant disease states (ASA IV).\n* Uncontrolled diabetes mellitus\n* Known or suspected non-compliance, drug or alcohol abuse.\n* Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant.\n* Participation in another study with investigational drug within the 30 days preceding and during the present study.\n* Previous enrolment into the current study.\n* Enrolment of the investigator, his\u002Fher family members, employees and other dependent persons.",{"count":96,"type":21},159,[52],"We are going to evaluate the difference between perioperative intravenous steroid supplementation, perioperative periarticular steroid supplementation, and standard anaesthesia protocols. We'll evaluate the outcome of patients with knee osteoarthritis who are undergoing Total Knee Arthroplasty to understand which of the three treatments give more benefits to the patient.",[100],"Total Knee Replacement",[102,103,104,105],"Knee","surgery","replacement","arthroplasty",{"date":81,"type":32},{"date":108,"type":32},"2020-07-01",{"date":110,"type":21},"2033-04-30",{"name":38,"class":39},""]