Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05936710

Improved Hemodynamic Tolerance of Intermittent Hemodialysis Sessions in Intensive Care Unite Using Citrate- vs Acetate-based Dialysate

Led by Centre Hospitalier de Bethune · Updated on 2026-05-08

48

Participants Needed

5

Research Sites

186 weeks

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

During intermittent hemodialysis (IHD), the occurrence of intradialytic hemodynamic instability (IHI) is frequent in ICU and impacted morbidity and mortality. Bicarbonate dialysate buffer improves hemodynamic tolerance compared to acetate dialysate buffer. However, bicarbonate dialysate buffer still contains a lower concentration of acetate, which could contribute to hemodynamic instability. Recently, citrate-based dialysate in bicarbonate hemodialysis instead of acetate have been proposed. They have the appropriate authorizations for routine use. The aim of this study is to compare acetate- vs citrate-based dialysate in terms of hemodynamic tolerance and effectiveness.

CONDITIONS

Official 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 63 18 years old
  • Patient hospitalized in an intensive care unit
  • Patient with acute renal failure defined by a KDIGO stage 63 1 and suspected non-obstructive
  • Patient at risk of per dialytic hypotension (capillary refill time 63 3 seconds and/or cardiovascular SOFA 63 1 and/or lactatemia > 2mmol/L)
  • Indication for Extra Renal Replacement Therapy with IHD.
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding woman
  • Known chronic renal insufficiency of any stage
  • Cardio-renal and hepato renal syndrome
  • Unstable hemodynamic state: refractory shock
  • Patient included in another interventional study likely to modify the hemodynamic state
  • Patient deprived of liberty
  • Patient under guardianship or curatorship
  • Patient not affiliated to a social security system

AI-Screening

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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

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Research Team

M

Martin GÉRARD

CONTACT

C

Christophe VINSONNEAU

CONTACT

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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