[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sodium-glucose-co-transporter-2-inhibitors\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sodium-glucose-co-transporter-2-inhibitors":138},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,53,83,114],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100645401","phase-2-sglt2i-effect-on-ptdm-development-and-kidney-allograft-function-in-non-diabetic-kidney-transplant-recipients-a-randomized-doubleblind-placebo-controlled-national-multicenter-trial-100645401",false,"NCT07682350","SGLT2i Effect on PTDM Development and Kidney Allograft Function in Non-diabetic Kidney Transplant Recipients: A Randomized, Doubleblind, Placebo Controlled, National Multicenter Trial","SGL-TX-PTDM: SGLT2i Effect on PTDM Development and Kidney Allograft Function in Kidney Transplant Recipients: A Randomized, Doubleblind, Placebo Controlled, National Multicenter Trial","SGL-TX-PTDM","Inclusion Criteria:\n\n* Obtained written informed consent\n* Male or female patients, age ≥ 18 years.\n* Non-diabetic KTR\n* Immunosuppressive must include Tacrolimus\n\nExclusion Criteria:\n\n* Patients who is treated (diet or antidiabetics) for diabetes type 1 or 2 before randomization\n* eGFR\\\u003C 25 ml\u002Fmin\u002F1.73m2 (before randomization)\n* Alanine aminotransferase (ALAT) \\> 3 x upper normal limit\n* Bilirubin \\> 2 x upper normal limit\n* Pregnancy\n* Positive plasma hCG\n* Breastfeeding\n* Known allergy towards SGLT2i or the content substance\n* Patients with chronic intestinal diseases, including inflammatory bowel diseases (e.g., Crohn's disease and ulcerative colitis) and structural conditions such as short bowel syndrome.","ALL","18 Years",{"count":20,"type":21},184,"ESTIMATED","INTERVENTIONAL",[24],"PHASE2","The goal of this clinical trial is to find out whether 12 months of treatment with the SGLT2 inhibitor Forxiga® (dapagliflozin 10 mg once daily), compared with placebo, can reduce the risk of developing post-transplant diabetes in kidney transplant recipients who do not have diabetes at the time of transplantation.\n\nThe main questions it aims to answer are:\n\n* Does Forxiga reduce the risk of developing post-transplant diabetes and prediabetes compared with placebo?\n* Does Forxiga help preserve the function of the transplanted kidney compared with placebo?\n* Is Forxiga safe for kidney transplant recipients who do not have diabetes?\n* Does Forxiga affect the occurrence of urinary tract infections, the amount of protein in the urine, and other kidney- and heart-related health measures compared with placebo?\n\nResearchers will compare Forxiga with a placebo (a look-alike tablet containing no active medicine) to see whether it can reduce the risk of post-transplant diabetes while maintaining kidney function and remaining safe to use.\n\nAdults who have recently received a kidney transplant and do not have diabetes may take part if they meet the study requirements.\n\nParticipants will be randomly assigned to receive either Forxiga or placebo once daily for 12 months. They will attend study visits 3, 6, and 12 months after joining the study. These visits will include health checks, blood tests, and urine tests. Neither the participants nor the study doctors will know which treatment each participant is receiving.",[27,28,29,30,31,32],"Kidney Transplant Recipient","Sodium Glucose Co-Transporter 2 Inhibitors","Non-Diabetic Patients","Randomized Controlled Trial (RCT)","Placebo Control Design","Post Transplant Diabetes Mellitus",[34,35,36,37,38,39,15],"SGLT2i","Kidney Transplant","Kidney Transplant Recipients","non-diabetic patients","Sodium-glucose Transporter 2 inhibitors","RCT","NOT_YET_RECRUITING","2026-06-26",{"date":43,"type":44},"2026-07-02","ACTUAL",{"date":46,"type":21},"2026-09-01",{"date":48,"type":21},"2029-10-01",{"name":50,"class":51},"Odense University Hospital","OTHER",3,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":61,"targetDuration":4,"studyType":22,"phases":63,"briefSummary":65,"conditions":66,"keywords":4,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":82},"100494256","phase-3-mechanisms-and-safety-of-sglt2-inhibition-in-peritoneal-dialysis-100494256","NCT05715814","meChANisms and sAfety of SGLT2 Inhibition in peRitoneal dialYsis","A Single Arm, Open Label, Pilot Study to Evaluate the Safety and Efficacy of Once Daily 25mg Empagliflozin in Patients on Peritoneal Dialysis With Residual Kidney Function","CANARY","Inclusion Criteria:\n\n* Signed and dated written informed consent.\n* Patients aged ≥18 years on PD with RKF defined as at least 250 cc of urine output per day (assessed via 24-hour urine collection) and a minimum measured GFR of 2 ml\u002Fmin\u002F1.73m2, as measured at least once in the last 3 months.\n* Stable PD prescription, as determined by investigators.\n* Stable dose of RAAS blockade if on a medication within this class for the last 30 days.\n\nExclusion Criteria:\n\n* Type 1 diabetes.\n* Recent (in the 30 days prior to screening) acute coronary syndrome or cerebrovascular event.\n* PD peritonitis within 30 days of screening.\n* History of organ transplant, including pancreas, pancreatic islet cells or kidney transplant.\n* Planned surgery\u002Fprocedures or radiologic investigations requiring contrast during the trial.\n* Pregnant, planning to become pregnant, or nursing an infant during the study period\n* History of any DKA event\n* Blood dyscrasias or any disorders causing hemolysis or unstable red blood cells (e.g., malaria, babesiosis, hemolytic anemia) at screening.\n* Women who are pregnant, nursing, or who plan to become pregnant whilst in the trial.\n* Alcohol or drug abuse within the 3 months prior to screening that would interfere with trial participation based on Investigator's judgement.\n* Use of SGLT2 inhibitor within 30 days prior to screening.\n* Intake of an investigational drug in another trial within 30 days prior to screening.\n* Patient not able to understand and comply with study requirements, based on Investigator's judgment.\n* Any other clinical condition that, based on Investigator's judgement, would jeopardize patient safety during trial participation or would affect the study outcome (e.g. immunocompromised patients, active malignancy, patients who might be at higher risk of developing genital or mycotic infections, patients with chronic viral infections, uncontrolled hypertension, cardiorenal and\u002For hepatorenal syndrome, severe hepatic impairments etc.).",{"count":62,"type":21},20,[64],"PHASE3","The primary aim of this study is to determine the safety and mechanisms of SGLT2 inhibition in individuals on peritoneal dialysis (PD) with residual kidney function (RKF).",[67,68,69,70,71],"Peritoneal Dialysis Complication","End Stage Kidney Disease","Sodium-glucose Co-transporter-2 Inhibitors","Kidney Dysfunction","Residual Kidney Function","RECRUITING","2026-04-30",{"date":75,"type":44},"2026-05-01",{"date":77,"type":44},"2024-09-01",{"date":79,"type":21},"2027-12-01",{"name":81,"class":51},"University Health Network, Toronto",1,{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":89,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":17,"minAge":91,"maxAge":18,"enrollmentInfo":92,"targetDuration":4,"studyType":22,"phases":94,"briefSummary":96,"conditions":97,"keywords":101,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":106,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":82},"100624098","phase-4-efficacy-and-safety-of-sodium-glucose-cotransporter-2-inhibitors-in-adolescents-with-early-stages-of-chronic-kidney-disease-100624098","NCT07405216","Efficacy and Safety of Sodium-Glucose Cotransporter-2 Inhibitors in Adolescents With Early Stages of Chronic Kidney Disease","Efficacy and Safety of Sodium-Glucose Cotransporter-2 Inhibitors in Adolescents With Persistent Albuminuria: A Randomized Controlled Clinical Trial","IECA-MEX","Inclusion Criteria:Age 14-18 years\n\nResidence in Aguascalientes\n\nPersistent albuminuria (ACR \\>30 and \\\u003C300 mg\u002Fg)\n\nEstimated glomerular filtration rate ≥60 mL\u002Fmin\u002F1.73 m²\n\nNo identifiable secondary cause (e.g., lupus, diabetes mellitus)\n\nRenal biopsy showing adaptive podocytopathy or perihilar focal segmental glomerulosclerosis -\n\nExclusion Criteria:\n\nHypoalbuminemia\n\nNephrotic syndrome\n\nPersistent macroalbuminuria (ACR \\>300 mg\u002Fg)\n\nSecondary causes of CKD, including congenital anomalies of the kidney and urinary tract or polycystic kidney disease -","14 Years",{"count":93,"type":21},200,[95],"PHASE4","Chronic kidney disease (CKD) is highly prevalent in the state of Aguascalientes, Mexico, particularly among adolescents and young adults. Epidemiologic and histologic studies suggest that this burden is largely driven by reduced nephron endowment of prenatal origin, leading to compensatory glomerular hyperfiltration, adaptive podocytopathy, and persistent albuminuria at early stages of disease.\n\nSodium-glucose cotransporter-2 inhibitors (SGLT2i) have demonstrated nephroprotective effects in adult populations with CKD, including reductions in albuminuria and slowing of disease progression, independent of diabetes status. However, no randomized controlled trials have evaluated the efficacy and safety of SGLT2 inhibitors in adolescents with early-stage CKD and persistent albuminuria.\n\nThis randomized, double-blind, placebo-controlled clinical trial aims to evaluate whether treatment with an SGLT2 inhibitor reduces albuminuria in adolescents aged 14 to 18 years with persistent microalbuminuria (albumin-to-creatinine ratio 30-300 mg\u002Fg) and preserved kidney function. Participants will be randomized in a 2:1 ratio to receive dapagliflozin 10 mg daily or placebo for six months. The primary outcome is the change in urinary albumin-to-creatinine ratio from baseline to six months. Secondary outcomes include changes in estimated glomerular filtration rate and safety outcomes.",[98,99,100,28],"Chronic Kidney Disease (Mild to Moderate)","Albuminuria","Adolescent",[102,103,104],"Chronic kidney disease","Persistent albuminuria","sodium glucose co-transporter 2 inhibitors","2026-04-22",{"date":107,"type":44},"2026-04-27",{"date":109,"type":44},"2026-04-23",{"date":111,"type":21},"2027-10-30",{"name":113,"class":51},"Centenario Hospital Miguel Hidalgo",{"id":115,"slug":116,"hasResults":11,"nctId":117,"briefTitle":118,"officialTitle":119,"acronym":4,"eligibilityCriteria":120,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":121,"enrollmentInfo":122,"targetDuration":4,"studyType":22,"phases":124,"briefSummary":126,"conditions":127,"keywords":4,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":82},"100546748","dapagliflozin-delays-the-loss-of-renal-function-in-peritoneal-dialysis-patients-100546748","NCT06398977","Dapagliflozin Delays the Loss of Renal Function in Peritoneal Dialysis Patients","Dapagliflozin Delays the Loss of Residual Renal Function in Patients Undergoing Peritoneal Dialysis: A Single-Center Randomized Open-Label Study","Inclusion Criteria:\n\n* Patients with PD duration between 1 month and 3 months.\n* Patients aged between 18 and 75 years.\n* Voluntary signing of informed consent.\n* Stable use of a maximum tolerated dose of RAAS inhibitors for one month if hypertension is present.\n* Daily urine output ≥ 400ml\u002Fday.\n* Stable PD prescription for one month.\n\nExclusion Criteria:\n\n* Pregnant and lactating women.\n* Patients with type 1 diabetes mellitus.\n* Patients with type 2 diabetes mellitus who have experienced diabetic ketoacidosis in the past.\n* Patients with chronic liver disease, including non-alcoholic fatty liver disease, cirrhosis, ALT \\> 120 IU\u002FL, and other clinically confirmed severe liver diseases.\n* Patients with more than 2 episodes of urinary tract infection in the past six months.\n* Patients with severe allergic reactions (rash or angioedema) to Dapagliflozin.\n* Patients using the following medications: rifampicin, phenytoin.\n* Patients with malignant tumors.\n* Patients who developed peritonitis within one month.\n* Patients undergoing combined hemodialysis treatment.\n* Patients with a willingness for kidney transplantation within six months.\n* Patients with a history of pancreatitis or pancreatic transplantation.\n* Patients who experienced acute coronary syndrome or cerebrovascular events within one month.\n* Hemoglobin level less than 90g\u002FL.","75 Years",{"count":123,"type":21},70,[125],"NA","This study aims to explore the role of dagliflozin in preserving the residual renal function(RRF) in peritoneal dialysis (PD) patients.",[67,128,69],"Renal Function Aggravated","2024-04-30",{"date":131,"type":44},"2024-05-03",{"date":133,"type":44},"2024-03-11",{"date":135,"type":21},"2026-12-31",{"name":137,"class":51},"Sichuan Academy of Medical Sciences","Sodium-glucose Co-transporter 2 Inhibitors"]