Groundbreaking Renal Assist Device Intervening to ENhance cardioThoracic Surgery Outcomes (NCT07017933) | Clinical Trial Compass
RecruitingNot Applicable
Groundbreaking Renal Assist Device Intervening to ENhance cardioThoracic Surgery Outcomes
United States, Poland124 participantsStarted 2025-07-16
Plain-language summary
Patients with renal insufficiency who undergo cardiac surgery with cardiopulmonary bypass (CPB) are at significant risk for exacerbation of renal dysfunction postoperatively. This in turn is associated with an increased risk of prolonged intensive care unit (ICU) length of stay, other comorbidities including surgical complications and 30-day mortality. Renal impairment is generally identified based on an increase in serum creatinine concentration and/or a certain magnitude decrease in estimated glomerular filtration rate (eGFR).
The JuxtaFlow® Renal Assist Device (RAD) is designed to sustain or enhance glomerular filtration perioperatively for patients with renal insufficiency by applying a mild controlled negative pressure to the collecting system via the renal pelvis, thereby increasing effective filtration pressure and reducing tubular pressure. This mechanism is designed to support the kidneys' functions during times of renal stress that would be associated with intrarenal edema, volume overload, increased venous pressure, and inflammatory response. By supporting renal function, specifically during the acute stress of CPB, JuxtaFlow holds promise to protect nephron function, decrease renal hypoxia, and provide multifactorial kidney function support to maintain their ability to manage future stress.
Who can participate
Age range22 Years – 85 Years
SexALL
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Inclusion criteria
✓. A candidate for elective or urgent on-pump coronary artery bypass grafting (CABG) and/or valvular surgery
✓. Female patients of childbearing potential must:
✓. have negative pregnancy test at the informed consent visit,
✓. be using previously initiated approved and effective contraception from the informed consent visit through completion of the study \*The only recommended contraception is condoms.
Exclusion criteria
✕. Any individual, or their legally authorized representative (LAR), who does not understand the requests and risks of participating in the clinical trial or is unable to give informed consent
✕. Pregnancy or lactation
What they're measuring
1
Mean Peak Percent Change in Serum Creatinine
Timeframe: 96 hours peri-operative
2
Incidence of Treatment-Emergent Adverse Events
Timeframe: From enrollment to post-operative day 30