[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100621014":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":22,"centralContacts":26,"locations":36,"responsibleParty":53,"collaborators":55,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":62,"sex":68,"minAge":10,"maxAge":10,"enrollmentInfo":69,"targetDuration":72,"studyType":73,"phases":10,"briefSummary":74,"conditions":75,"keywords":80,"overallStatus":84,"whyStopped":10,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"University of Alberta","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients",null,"Any patients admitted to the ICU and required CRRT",[13],"Device: continuous renal replacement therapy",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","continuous renal replacement therapy","We will include any critically ill patient admitted to an intensive care unit requiring dialysis",[9],[21],"CRRT",[23],{"name":24,"affiliation":5,"role":25},"Oleksa Rewa","PRINCIPAL_INVESTIGATOR",[27,32],{"name":28,"role":29,"phone":30,"phoneExt":10,"email":31},"Oleksa Rewa, MD MSc FRCPC","CONTACT","178026332850","rewa@ualberta.ca",{"name":33,"role":29,"phone":34,"phoneExt":10,"email":35},"Fadi Hammal, MD MSc","15879907454","hammal@ualberta.ca",[37],{"facility":5,"status":10,"city":38,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Edmonton","Alberta","T6G 2G3","Canada","CA",{"type":44,"coordinates":45},"Point",[46,47],-113.46871,53.55014,{"lat":47,"lon":46},[50],{"name":51,"role":29,"phone":52,"phoneExt":10,"email":35},"Fadi Hammal","5879907454",{"type":54,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[56,58],{"name":57,"class":6},"University of Alabama at Birmingham",{"name":59,"class":6},"University of Zagreb","100621014","insights-into-the-continuous-renal-replacement-therapy-to-critical-ill-patients-100621014",false,"NCT07365111","Insights Into the Continuous Renal Replacement Therapy to Critical Ill Patients","Insights Into the Characteristics, Prescription and Delivery of Continuous Renal Replacement Therapy to Critical Ill Patients - The iCRRT Data Registry","iCRRT","Inclusion Criteria:\n\n1. Admission to an intensive care unit\n2. CRRT therapy\n\nExclusion Criteria:\n\n1. End-stage kidney disease\n2. CRRT \\\u003C24 hours","ALL",{"count":70,"type":71},100000,"ESTIMATED","90 Days","OBSERVATIONAL","This is a multinational, prospective, observational study designed to characterize patient demographics, prescription parameters, and process measures of continuous renal replacement therapy (CRRT) in intensive care units (ICUs) worldwide. The study aims to examine similarities and differences in CRRT practices and outcomes among critically ill adult patients across a global network of medical centers.\n\nThe goal is to develop a large, comprehensive repository of data on CRRT practices and outcomes. This repository will enable characterization of variation in standard CRRT practices across medical centers. Natural variability in practice patterns-both between and within centers-will provide an opportunity to compare outcomes associated with different approaches and to generate high-quality preliminary data to inform future interventional trials.\n\nPrimary Objective\n\n\\- To describe global patient characteristics, CRRT modalities, and clinical outcomes among patients receiving CRRT.\n\nSecondary Objectives\n\n* To compare clinical outcomes across geographic regions and CRRT modalities.\n* To identify patient-level and practice-level predictors of outcomes.\n* To assess the impact of comorbid conditions (e.g., diabetes mellitus) on CRRT outcomes.\n\nExploratory Objectives\n\n* To evaluate long-term renal outcomes and patient-reported quality of life.\n* To explore health economics and resource utilization related to CRRT.\n\nStudy Population All patients receiving CRRT as part of routine clinical care in the ICU at participating centers will be eligible for inclusion.\n\nData Collection The study will support an epidemiological assessment of patients undergoing CRRT, including, but not limited to, demographics, underlying disease states, severity of illness, physiological support, indications for CRRT, and clinical outcomes. Outcomes of interest include ICU and hospital mortality, ICU and hospital length of stay, and renal recovery.",[76,77,78,79],"Continuous Renal Replacement Therapy (CRRT)","Acute Kidney Injury","Renal Dialysis","Critical Illness",[81,82,77,83],"Continue Renal Replacement Therapy","Dialysis","Intensive Care Unit","NOT_YET_RECRUITING","2026-05-28",{"date":87,"type":88},"2026-06-01","ACTUAL",{"date":90,"type":71},"2026-07-01",{"date":92,"type":71},"2036-12-31",{"name":5,"class":6},1]