[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100390951":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":18,"centralContacts":22,"locations":32,"responsibleParty":52,"collaborators":54,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":63,"eligibilityCriteria":64,"healthyVolunteers":59,"sex":65,"minAge":66,"maxAge":67,"enrollmentInfo":68,"targetDuration":71,"studyType":72,"phases":10,"briefSummary":73,"conditions":74,"keywords":10,"overallStatus":35,"whyStopped":10,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},{"fullName":5,"class":6},"University of Calgary","OTHER",[8,12,15],{"label":9,"type":10,"description":11,"interventionNames":10},"Registry Group",null,"Patients who sustain and present with a PLI injury will have two options for participating in the study. This first arm will evaluate clinical presentations, patient demographic, treatment methods and baseline patient-rated and radiographic outcomes. However, no research-related follow up visits will be conducted. Ongoing data from these participants will be collected from chart reviews of clinical follow-ups alone.",{"label":13,"type":10,"description":14,"interventionNames":10},"Prospective Group","Participants who choose to enroll in the prospective arm will experience the same baseline data collection as those in the registry, with the addition of research-related follow up appointments that will allow research staff to measure and assess patient-rated and clinical outcomes, such as questionnaires and range of motion data.",{"label":16,"type":10,"description":17,"interventionNames":10},"Retrospective Group","In this group, a chart review will be conducted to identify previously treated patients with perilunate injuries. Once identified, the patient will be contacted and ask if they are willing to come in for a long-term follow up visit where clinical, patient-rated, and radiographic data will be collected. If patients are unwilling to attend a long-term visit, our analysis will still include data collected from their chart reviews and electronic questionnaires.",[19],{"name":20,"affiliation":5,"role":21},"Neil J White, MD, FRCSC","PRINCIPAL_INVESTIGATOR",[23,28],{"name":24,"role":25,"phone":26,"phoneExt":10,"email":27},"Adina Tarcea, BMSc","CONTACT","4039563687","adina.tarcea@ucalgary.ca",{"name":29,"role":25,"phone":30,"phoneExt":10,"email":31},"Sarah L Reitzel, BN","403-956-1971","slreitze@ucalgary.ca",[33],{"facility":34,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"South Health Campus","RECRUITING","Calgary","Alberta","T3M1M4","Canada","CA",{"type":42,"coordinates":43},"Point",[44,45],-114.08529,51.05011,{"lat":45,"lon":44},[48,50],{"name":49,"role":25,"phone":26,"phoneExt":10,"email":10},"Tina Samuel, MBBS",{"name":51,"role":21,"phone":10,"phoneExt":10,"email":10},"Neil J White, MD",{"type":53,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[55],{"name":56,"class":6},"University of Alberta","100390951","the-canadian-prospective-pragmatic-perilunate-outcomes-trial-100390951",false,"NCT04370626","The Canadian Prospective Pragmatic Perilunate Outcomes Trial","The Canadian Prospective Pragmatic Perilunate Outcomes Trial (The C3PO Trial)","C3PO","Inclusion Criteria:\n\n* The subject is 14 years of age or older\n* The subject has been clinically diagnosed with a perilunate injury\n* The subject is willing to adhere to the study protocol including required post-operative therapy, all scheduled follow-up visits, evaluations, and questionnaires (if applicable).\n\nExclusion Criteria:\n\nThere will be no limiting exclusion criteria.","ALL","14 Years","120 Years",{"count":69,"type":70},450,"ESTIMATED","10 Years","OBSERVATIONAL","This is a unique three-fold prospective and retrospective study. With this approach, all previous and current PLIs presented at participating study sites will have the potential to be included in the study. Our goal is to collect all relevant injury and surgical parameters of the Perilunate spectrum. The investigators plan to identify each hospital within Canada that normally treats PLIs and to record injury and demographic information on each PLI that occurs in this country over a two to three-year period. Our protocol includes scheduled two, five, and 10-year follow-up intervals.",[75,76,77,78],"Wrist Injuries","Carpal Bone Fracture","Dislocation of Wrist","Trauma","2022-11-18",{"date":81,"type":82},"2022-11-23","ACTUAL",{"date":84,"type":82},"2020-09-01",{"date":86,"type":70},"2026-12-31",{"name":5,"class":6},1]