[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100643525":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":28,"centralContacts":32,"locations":42,"responsibleParty":59,"collaborators":62,"id":66,"slug":67,"hasResults":68,"nctId":69,"briefTitle":70,"officialTitle":70,"acronym":71,"eligibilityCriteria":72,"healthyVolunteers":68,"sex":73,"minAge":74,"maxAge":21,"enrollmentInfo":75,"targetDuration":21,"studyType":78,"phases":79,"briefSummary":81,"conditions":82,"keywords":86,"overallStatus":95,"whyStopped":21,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":105},{"fullName":5,"class":6},"University of Washington","OTHER",[8,14,17],{"label":9,"type":10,"description":11,"interventionNames":12},"Ultrafiltration sessions for 4 weeks","ACTIVE_COMPARATOR","Two ultrafiltration sessions per week plus pharmacist guided tapering of blood pressure medications in addition to the regular thrice weekly hemodialysis treatments.",[13],"Procedure: Ultrafiltration",{"label":15,"type":10,"description":11,"interventionNames":16},"Ultrafiltration sessions for 8 weeks",[13],{"label":18,"type":19,"description":20,"interventionNames":21},"Control arm, no ultrafiltration sessions","NO_INTERVENTION","Participant receives only their regularly scheduled thrice weekly hemodialysis treatments.",null,[23],{"type":24,"name":25,"description":26,"armGroupLabels":27,"otherNames":21},"PROCEDURE","Ultrafiltration","Ultrafiltration for 4 or 8 weeks compared to no ultrafiltration.",[9,15],[29],{"name":30,"affiliation":5,"role":31},"Bryan Kestenbaum, MD, MS","PRINCIPAL_INVESTIGATOR",[33,38],{"name":34,"role":35,"phone":36,"phoneExt":21,"email":37},"Luisa Rios-Avila","CONTACT","206-258-9325","lrios1@uw.edu",{"name":39,"role":35,"phone":40,"phoneExt":21,"email":41},"Ernest Ayers, MSPH","206-685-1423","ayerse@uw.edu",[43],{"facility":44,"status":21,"city":45,"state":46,"zip":47,"country":48,"countryCode":49,"cosmosGeoPoint":50,"geoPoint":55,"contacts":56},"Northwest Kidney Centers","Seattle","Washington","98112","United States","US",{"type":51,"coordinates":52},"Point",[53,54],-122.33207,47.60621,{"lat":54,"lon":53},[57],{"name":34,"role":35,"phone":58,"phoneExt":21,"email":37},"2062589325",{"type":31,"investigatorFullName":60,"investigatorTitle":61,"investigatorAffiliation":5,"oldNameTitle":21,"oldOrganization":21},"Bryan Kestenbaum","Professor, Medicine - Nephrology",[63],{"name":64,"class":65},"National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)","NIH","100643525","dry-weight-reduction-intervention-via-extra-ultrafiltration-100643525",false,"NCT07637110","Dry Weight Reduction Intervention Via Extra Ultrafiltration","DRIVE-UF","Inclusion Criteria:\n\n* Receiving thrice weekly in-center hemodialysis treatments for end stage kidney disease for at least four weeks and clinical suspicion of volume excess based on either:\n\n  1. Persistent hypertension defined by three consecutive pre-dialysis systolic blood pressures ≥140 mmHg or three consecutive pre-dialysis systolic blood pressures 130-140 mmHg plus use of at least two anti-hypertensive medications that can be tapered.\n\n     OR\n  2. Symptoms of congestion defined by a 12-item Kidney Modified Kansas City Cardiomyopathy Questionnaire (KM-KCCQ) score \\\u003C75.\n\n     Exclusion Criteria:\n* Age \\\u003C18 years\n* Receiving hemodialysis treatments for acute kidney injury\n* Receiving hemodialysis treatments for less than four weeks\n* Planned switch to peritoneal or home dialysis within next three months\n* Current or planned incremental hemodialysis (less than 3 treatments per week)\n* Current or planned intensive hemodialysis (four or more treatments per week)\n* Scheduled kidney transplantation\n* Major cardiovascular or bleeding event within previous 90 days\n* Receiving chemotherapy or radiation treatment for cancer\n* History of cirrhosis with ascites\n* Inability to complete 24-hour ambulatory blood pressure measurement\n* Wheelchair dependance or other inability to complete six-minute walk test\n* Pre-dialysis systolic blood pressure \\\u003C100 mmHg\n* Scheduled use of midodrine with hemodialysis treatments\n* History of non-adherence with dialysis treatments\n* Pregnancy\n* Institutionalized\n* Current or pending enrollment in hospice care\n* Inappropriate for enrollment based on investigator or nephrologist discretion","ALL","18 Years",{"count":76,"type":77},120,"ESTIMATED","INTERVENTIONAL",[80],"NA","Most patients who receive hemodialysis treatments have excess fluid in their body that has slowly built up over the course of kidney disease. This extra fluid is the main cause of high blood pressure in dialysis and leads to stress on the heart and lungs.that causes debilitating symptoms and frequent hospitalizations.\n\nThis trial will test whether a focused program of 4 or 8 weeks of extra ultrafiltration treatments can remove most of this extra fluid. We believe that getting rid of large amounts of extra fluid will result in sustained improvements in blood pressure and symptoms. Ultrafiltration is a gentler type of dialysis that removes fluid but does not clean the blood.",[83,84,85],"Fluid Accumulation","Blood Pressure Management","End Stage Renal Disease (ESRD)",[87,88,89,90,91,92,93,94],"ESRD","Volume overload","Fluid accumulation","End stage renal disease","Congestion","Chronic dialysis","Blood Pressure (High)","Blood pressure management","NOT_YET_RECRUITING","2026-06-03",{"date":98,"type":99},"2026-06-09","ACTUAL",{"date":101,"type":77},"2026-06",{"date":103,"type":77},"2030-11",{"name":5,"class":6},1]