Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05936710

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

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

Follow-up

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

Loading map...

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

Similar Trials

Using Intradialytic Blood Pressure Slopes to Guide Fluid Rem...

End Stage Renal Disease

Actively Recruiting

1 location

The Predictive Value of the Inferior Vena Cava Collapsibilit...

End-Stage Renal Disease Requiring Haemodialysis

Actively Recruiting

1 location

The Value of Pleth Variability Index in Predicting Hypotensi...

Hypotension and Shock

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here