[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"fracture-dislocation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:fracture-dislocation":77},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,53],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":12,"acronym":4,"eligibilityCriteria":13,"healthyVolunteers":10,"sex":14,"minAge":15,"maxAge":4,"enrollmentInfo":16,"targetDuration":4,"studyType":19,"phases":20,"briefSummary":22,"conditions":23,"keywords":29,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100568224",false,"NCT06678438","Brachial Plexus Nerve Block Versus Haematoma Block for Closed Reduction of Distal Radius Fracture in Adults - The BLOCK Trial. A Multicentre Randomised Controlled Trial.","Inclusion Criteria:\n\n* Adults (age ≥ 18 years) with a distal radius fracture in need of closed reduction\n\nExclusion Criteria:\n\n* Patients who would never qualify for surgery according to local guidelines\n* Lack of informed consent\n* No Danish Central Person Register (CPR) number\n* Allergies to the trial medication\n* Distal radius fracture initially deemed to require surgery regardless of the outcome of the closed reduction\n* Open fractures (fracture-related wound requiring sutures)\n* Other fractures on the same extremity ((NOT including distal ulna fracture(s))\n* Bilateral distal radius fractures both requiring closed reduction\n* Concomitant medical or surgical condition taking priority over the closed reduction of the distal radius fracture.","ALL","18 Years",{"count":17,"type":18},1716,"ESTIMATED","INTERVENTIONAL",[21],"PHASE4","The aim of the project is to evaluate the beneficial and harmful effects of an ultrasound-guided brachial plexus nerve block for patients with a distal radius (wrist) fracture in the need of realignment of fractured bone endings without cutting the skin (closed reduction), in comparison to a haematoma block, which is standard care in Denmark.\n\nEvery participant will receive one of the following types of anaesthesia for the realignment of the wrist fracture:\n\n1. A nerve block of the arm (plexus brachialis block)\n2. A haematoma block, which is the current standard anaesthesia in the emergency departments.",[24,25,26,27,28],"Distal Radius Fractures","Fracture Dislocation","Fracture Dislocation of Upper Limb Joint","Colles' Fracture","Closed Reduction of Fracture and Application of Plaster Cast",[30,31,32,33,34,35,36,37,38,39],"Lidocaine","Local anaesthesia","Regional anaesthesia","Peripheral nerve block","Brachial plexus block","Lateral infraclavicular block","Axillary plexus block","Distal radius fracture","Colles' fracture","Wrist fracture","RECRUITING","2025-06-12",{"date":43,"type":44},"2025-06-17","ACTUAL",{"date":46,"type":44},"2024-12-10",{"date":48,"type":18},"2027-04",{"name":50,"class":51},"Nordsjaellands Hospital","OTHER",1,{"id":54,"slug":4,"hasResults":10,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":10,"sex":14,"minAge":59,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":62,"phases":4,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":52},"100493346","NCT05703958","Exactech Proximal Humerus Fracture Plate System Post Market Clinical Follow-up","An Open Label, Multi-Center, Retrospective and Prospective Evaluation of Equinoxe Proximal Humerus Fracture Plates Clinical and Radiographic Outcomes","Inclusion Criteria:\n\n* Patient is indicated to receive Equinoxe Proximal Humerus Fracture Plate or has previously underwent primary surgery with Equioxe Proximal Humerus Fracture Plate\n* Patient is willing to participate by complying with pre- and postoperative visit requirements\n* Patient is willing to agree to be followed for up to 10 years following their index surgery\n* Patient is willing and able to review and sign a study informed consent form\n\nExclusion Criteria:\n\n* Osteomyelitis of the proximal humerus or scapula\n* Inadequate or malformed bone that precludes adequate support or fixation of the prosthesis\n* Patient's age, weight, or activity level would cause the surgeon to expect early failure of the system\n* The patient is unwilling or unable to comply with the post-operative care instructions\n* Alcohol, drug, or other subtance abuse\n* Any disease state that could adversaly affect the function or longevity of the implant\n* Patient is pregnant\n* Patient is a prisoner\n* Patient has a physical or mental condition that would invalidate the results","21 Years",{"count":61,"type":18},151,"OBSERVATIONAL","The objective of this study is to collect and evaluate long-term clinical outcomes data in order to better understand the safety and performance of the Equinoxe Proximal Humerus Fracture Plates over time. This study will follow subjects for a period of up to 10 years post-surgery.",[65,25,66],"Proximal Humeral Fracture","Non-Union Fracture","2024-10-23",{"date":69,"type":44},"2024-10-24",{"date":71,"type":44},"2023-04-19",{"date":73,"type":18},"2034-09-30",{"name":75,"class":76},"Exactech","INDUSTRY",""]