Actively Recruiting
Improved Hemodynamic Tolerance of Intermittent Hemodialysis Sessions in Intensive Care Unit Using Citrate- vs Acetate-based Dialysate
Led by Centre Hospitalier de Bethune · Updated on 2026-05-08
48
Participants Needed
5
Research Sites
N/A
Total Duration
On this page
Sponsors
C
Centre Hospitalier de Bethune
Lead Sponsor
C
CHU de Lille
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are comparing two types of dialysate used during intermittent hemodialysis (IHD) sessions in intensive care units (ICU) to see which one better supports stable blood pressure. The study focuses on patients with acute kidney failure who are at risk for intradialytic hypotension, a common problem during dialysis that can affect recovery and survival. This trial evaluates citrate-based dialysate against the more common acetate-based dialysate to determine which provides better hemodynamic tolerance and dialysis effectiveness. Participants will be randomly assigned to receive IHD using either acetate-based or citrate-based dialysate. Both types are approved for routine use, but citrate dialysate may reduce episodes of low blood pressure during dialysis. The study will monitor treatment sessions up to 28 days, comparing how often hypotension occurs and other health outcomes like mortality, ICU stay length, kidney function recovery, and dialysis efficiency. Throughout the study, patients will undergo regular assessments including vital signs, blood tests for kidney function and electrolytes, and measurement of dialysis adequacy. Researchers will track the number of dialysis sessions with hemodynamic instability and evaluate recovery markers such as urine output and organ function scores. Safety and effectiveness will be observed during the ICU stay and up to day 28, with data collected on ventilation use, medication needs, and hospital length of stay.
CONDITIONS
Brief Title
Improved Hemodynamic Tolerance of Intermittent Hemodialysis Sessions in Intensive Care Unite Using Citrate- vs Acetate-based Dialysate
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient 18 years or older
- Hospitalized in an intensive care unit
- Acute kidney failure defined by KDIGO stage 1 or higher and suspected to be non-obstructive
- At risk of low blood pressure during dialysis indicated by capillary refill time 3 seconds or more and/or cardiovascular SOFA score 1 or higher and/or lactate level above 2 mmol/L
- Indication for intermittent hemodialysis as extra renal replacement therapy
You will not qualify if you...
- Pregnant or breastfeeding women
- Known chronic kidney disease of any stage
- Cardio-renal or hepato-renal syndrome
- Unstable hemodynamic state such as refractory shock
- Participation in another interventional study that may affect hemodynamics
- Patients deprived of liberty
- Patients under guardianship or curatorship
- Patients not affiliated with a social security system
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 28 days
Participants receive intermittent hemodialysis sessions using either citrate- or acetate-based dialysate as assigned.
Multiple dialysis sessions as prescribed during ICU stay within 28 days
Duration - Up to 28 days
Participants are monitored for hemodynamic tolerance and other health outcomes up to 28 days after starting dialysis treatment.
Regular assessments during ICU stay up to day 28
Trial Site Locations
Total: 5 locations
1
Centre Hospitalier Béthune
Béthune, France, 62408
Actively Recruiting
2
CHU
Caen, France
Actively Recruiting
3
Centre Hospitalier Universitaire de Dijon
Dijon, France
Actively Recruiting
4
CHRU Nancy
Nancy, France
Actively Recruiting
5
CHU de ROUEN
Rouen, France, 59507
Not Yet Recruiting
Research Team
M
Martin GÉRARD
C
Christophe VINSONNEAU
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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