Clinical trial Recruiting at 4 sites Interventional Ages 18 and up

Comparing citrate and acetate dialysate for better hemodynamic stability during hemodialysis in ICU patients

Official title: Improved Hemodynamic Tolerance of Intermittent Hemodialysis Sessions in Intensive Care Unite (ICU) Using Citrate- vs Acetate-based Dialysate

Run by Centre Hospitalier de Bethune · NCT05936710 · Data updated 2026-11-12

This study is testing whether using citrate instead of acetate in dialysis can help ICU patients feel more stable and avoid low blood pressure during their treatment.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment48 (estimated)
SponsorCentre Hospitalier de Bethune
Research network
Locations5 sites (Béthune and 4 other locations)
StatusRecruiting
StartedDecember 7, 2023
Main results expectedJuly 2027
Study endsJuly 2027
Registry record updatedMay 8, 2026
Trial IDNCT05936710 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 and older who are hospitalized in an intensive care unit with acute renal failure and at risk of per dialytic hypotension.

Probably not a fit

Patients with chronic renal insufficiency, unstable hemodynamic states, or those who are pregnant or breastfeeding may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to evaluate the hemodynamic tolerance and effectiveness of citrate-based dialysate compared to acetate-based dialysate during intermittent hemodialysis in patients hospitalized in intensive care units. It focuses on patients experiencing intradialytic hypotension, a common complication that can lead to increased morbidity and mortality. By using citrate-based dialysate, the study seeks to determine if it can provide better stability and outcomes for patients undergoing hemodialysis. The study will involve patients who meet specific criteria related to acute renal failure and risk of hypotension.

Why it matters

Potential benefit: If successful, this study could lead to improved hemodynamic stability during hemodialysis, reducing complications and enhancing patient outcomes.

How similar studies have gone: While the use of citrate-based dialysate is a newer approach, previous studies have indicated potential benefits, but this specific comparison is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient ≥ 18 years old
* Patient hospitalized in an intensive care unit
* Patient with acute renal failure defined by a KDIGO stage ≥ 1 and suspected non-obstructive
* Patient at risk of per dialytic hypotension (capillary refill time ≥ 3 seconds and/or cardiovascular SOFA ≥ 1 and/or lactatemia \> 2mmol/L)
* Indication for Extra Renal Replacement Therapy with IHD.

Exclusion Criteria:

* 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

Where it's running

  • Centre Hospitalier Béthune
    Béthune, France
    Recruiting
  • Chu
    Caen, France
    Recruiting
  • Centre Hospitalier Universitaire de Dijon
    Dijon, France
    Recruiting
  • CHRU Nancy
    Nancy, France
    Recruiting
  • CHU de ROUEN
    Rouen, France
    Not yet recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.