[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hemodialysis-catheter\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hemodialysis-catheter":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,55],{"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":30,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100624031","phase-4-low-dose-apixaban-added-to-standard-heparin-lock-versus-heparin-lock-alone-to-prevent-tunneled-hemodialysis-catheters-dysfunction-apicath-hd-100624031",false,"NCT07404345","Low-Dose Apixaban Added to Standard Heparin Lock Versus Heparin Lock Alone to Prevent Tunneled Hemodialysis Catheters Dysfunction (APICATH-HD)","Efficacy of Low-Dose Apixaban Added to Standard Heparin Lock to Prevent Dysfunction of Tunneled Hemodialysis Catheters: A Randomized, PROBE, Parallel-Grupo Trial.","APICATH-HD","Inclusion Criteria:\n\n* Age ≥18 years with end-stage kidney disease (CKD stage 5) receiving maintenance hemodialysis or initiating hemodialysis.\n* Recently placed tunneled, double-lumen central venous hemodialysis catheter (tunneled CVC) in place for ≥8 days, with a post-placement radiograph confirming adequate tip position.\n* Permitted catheter insertion sites: right internal jugular, left internal jugular, right femoral, or left femoral vein.\n* Adequate initial catheter function, defined as ability to achieve the prescribed extracorporeal blood flow (suggested ≥300 mL\u002Fmin) for ≥8 days after catheter placement.\n* Conventional in-center hemodialysis schedule (2-3 sessions\u002Fweek) at the study unit, with expected ability to complete follow-up for up to 24 months.\n* Written informed consent provided.\n* Willingness to receive only the protocol-assigned antithrombotic prophylaxis and to avoid non-study systemic anticoagulants or antiplatelet agents during the study period.\n\nExclusion Criteria:\n\n* Non-tunneled hemodialysis catheter, subclavian catheter, or intracaval catheter placement not consistent with the protocol (e.g., catheter located in the SVC\u002FIVC without a subcutaneous tunnel, or catheter location\u002Fsite not permitted by the study).\n* Tunneled catheter placed \\\u003C8 days before randomization or radiographically confirmed catheter tip malposition at screening.\n* Active bleeding; active peptic ulcer disease; or clinically significant gastrointestinal bleeding within the past 30 days; uncorrectable INR \\>1.5; platelet count \\\u003C100,000\u002FµL.\n* High bleeding risk (HAS-BLED score \\>3) or major bleeding that is active or recent.\n* Known coagulopathy; history of heparin-induced thrombocytopenia (HIT); or allergy\u002Fhypersensitivity to heparin, citrate, or rt-PA (alteplase).\n* Severe hepatic impairment (e.g., Child-Pugh class C), clinically significant liver dysfunction that contraindicates DOAC therapy, or ongoing hemodialysis with regional citrate anticoagulation that cannot be modified per protocol.\n* Active catheter exit-site infection or bloodstream infection\u002Fbacteremia at the time of randomization.\n* Concomitant use of other systemic anticoagulants (e.g., warfarin, low-molecular-weight heparin, other DOACs) or high-intensity antiplatelet therapy (e.g., dual antiplatelet therapy).\n* Pregnancy or breastfeeding.\n* Women of childbearing potential who are unwilling to use a highly effective contraception method during the study and for 48 hours after the last dose of study medication.\n* Life expectancy \\\u003C6 months, current palliative\u002Fhospice care, or planned kidney transplant within ≤3 months.\n* Concurrent participation in another clinical trial that could interfere with the study interventions or outcomes.\n* Venography demonstrating significant venous stenosis involving the superior vena cava (SVC) or inferior vena cava (IVC).","ALL","18 Years",{"count":20,"type":21},54,"ESTIMATED","INTERVENTIONAL",[24],"PHASE4","This randomized, single-center, PROBE trial evaluates whether adding low-dose apixaban (2.5 mg orally every 12 hours) to standard intraluminal heparin lock prolongs primary functional patency of tunneled hemodialysis catheters compared with standard heparin lock alone. Adult patients on hemodialysis with a recently implanted, functioning tunneled catheter (≥8 days) will be randomized 1:1 and followed up to 24 months (or until catheter loss). Primary outcome is time to first intervention for catheter dysfunction or definitive catheter loss. Secondary outcomes include primary-assisted and secondary patency, thrombotic dysfunction, rescue procedures, catheter-related infection, bleeding (ISTH), and mortality. Outcomes adjudication will be blinded.",[27,28,29],"Hemodialysis Access Failure","Kidney Disease, End-Stage","Hemodialysis Catheter",[31,32,33,34,35,36,37,38,39,40,41],"Hemodialysis","Tunneled central venous catheter","Catheter dysfunction","Catheter Failure","Catheter thrombosis","Apixaban","Heparin lock","End-stage kidney disease","Vascular access","Anticoagulation","PROBE trial","NOT_YET_RECRUITING","2026-02-12",{"date":45,"type":46},"2026-02-17","ACTUAL",{"date":48,"type":21},"2026-03-01",{"date":50,"type":21},"2028-09-01",{"name":52,"class":53},"Hospital Civil de Guadalajara","OTHER",1,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":62,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":63,"targetDuration":4,"studyType":22,"phases":65,"briefSummary":67,"conditions":68,"keywords":70,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":4},"100589861","the-effect-of-arteriovenous-fistula-care-training-given-to-hemodialysis-patients-on-quality-of-life-comfort-and-self-care-behaviours-100589861","NCT06959914","The Effect of Arteriovenous Fistula Care Training Given to Hemodialysis Patients on Quality of Life, Comfort and Self-Care Behaviours","Fistula care","Inclusion Criteria:\n\n* -Volunteering to participate in the research,\n* Speaking Turkish.\n* 18 years of age or older\n* Having AVF\n* Receiving HD treatment 3 times a week for at least 6 months\n* Not having cognitive and mental problems that prevent participation in the study\n\nExclusion Criteria:\n\n* Not consenting to participate in the study\n\n  * Being a diagnosed psychiatric individual,\n  * Having a visual, hearing, speech, physical or mental disability,\n  * Being incomplete in their education.",true,{"count":64,"type":21},60,[66],"NA","This study will be conducted to evaluate the effect of Arterio-Venous Fistula (AVF) care training given to hamodialysis patients on quality of life, comfort and self-care behaviours. Patient education is one of the practices that help patients to gain self-care behaviours as well as reducing the cost of health expenditures. Nurses are health professionals who play an important role in patient education. Nurses provide patient education by using different materials. These materials can sometimes be mobile phones, videos, web-based applications, sometimes face-to-face interviews with patients, brochures or written materials. In this study, a training programme for AVF care will be developed. In addition, it is expected that the AVF care training to be given to HD patients will increase the quality of life and comfort areas, and increase the awareness and well-being levels of patients in self-care behaviours. The effectiveness of the study will be expanded by presenting the results of the research as a paper in an international comprehensive congress. An article of the study will be published in a journal scanned in international indexes and will be included in the literature.",[69,29],"Hemodialysis Patient",[71,72,73,74,31,75],"Arteriovenous Fistula","Qualitiy of life","Comfort","Self-care","Hemodialysis access","2025-05-07",{"date":78,"type":46},"2025-05-13",{"date":80,"type":21},"2025-09",{"date":82,"type":21},"2026-09",{"name":84,"class":53},"Kafkas University"]