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CompletedNCT05209230MS-CRRTUpdated Jan 8, 2026

Is Myocardial Stunning Induced by Continuous Renal Replacement Therapy a Reality in Critically Ill Patients?

An interventional study of Continuous renal replacement therapy and Control group in Acute Kidney Injury KDIGO 3, Continuous Renal Replacement Therapy Initiated by the Clinician in Charge Without Emergency and Myocardial Stunning, sponsored by Hospices Civils de Lyon. Completed at 3 sites in France. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2026-01-08.

Sponsored by Hospices Civils de Lyon · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
18 Years to 90 Years
Sex
All
01

Study summary

Myocardial stunning during chronic intermittent hemodialysis is a well-described phenomenon. Little case series of patients presenting myocardial stunning during renal replacement therapy for acute kidney injury in critically ill patients are reported, with intermittent hemodialysis and continuous renal replacement therapy. However, the small sample sizes and the absence of a control arm limit their interpretation, mainly whether the myocardial stunning may be related to cardiac loading conditions variations and whether it may impact the hemodynamic.

The investigator hypothesize that myocardial stunning induced by renal replacement therapy is frequent, independent from cardiac loading conditions and associated with peripheral hypoperfusion.

02

Conditions studied

  • Acute Kidney Injury KDIGO 3
  • Continuous Renal Replacement Therapy Initiated by the Clinician in Charge Without Emergency
  • Myocardial Stunning

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Keywords

  • Acute kidney injury,
  • continuous renal replacement therapy
  • myocardial stunning
  • regional wall motion abnormalities
  • 2D speckle tracking echocardiography
03

In context

Acute Kidney Injury

1,595 studies on the registry are indexed under Acute Kidney Injury; 371 are open to participants now.

This study's enrollment of 42 is below the median of 100 across 763 interventional studies indexed under Acute Kidney Injury.

Browse Acute Kidney Injury studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,826 studies on the registry; 439 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age > 18 years old
  • Acute Kidney Injury grade 3 (KDIGO)
  • Indication for renal replacement therapy for the clinician in charge

Exclusion criteria

Exclusion Criteria:

  • Emergency indication to renal replacement therapy (pH\<7.15, Kaliemia > 6mmol/L, refractory pulmonary oedema)
  • Poor echogenicity with speckle tracking analysis failure
  • Chronic hemodialysis
  • Extra corporeal membrane oxygenation, left ventricular assist device.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
42 participants (actual)

Study arms

  • Experimental
    Continuous renal replacement therapy arm

    Echocardiographic evaluation (with 2D speckle tracking analysis of left ventricular segmental function) 1 hour before and 3 hours after the initiation of continuous renal replacement therapy (continuous veno venous hemofiltration) initiation

    Procedure: Continuous renal replacement therapy

  • Other
    Control arm

    Two echocardiographic evaluations (with 2D speckle tracking analysis of left ventricular segmental function) at an interval of 4 hours, before the continuous renal replacement therapy initiation.

    Other: Control group

Interventions

  • ProcedureContinuous renal replacement therapy

    Continuous renal replacement therapy (veno venous hemofiltration) without net ultrafiltration, through a dedicated central venous catheter

  • OtherControl group

    Continuous renal replacement therapy is differed from 6 hours to allowed 2 control echocardiographic evaluations

06

What researchers measure

Primary outcomes

  1. Number of segment of the left ventricle with regional wall motion abnormalities

    Numbers of segments of the left ventricle (by patient) with a decrease greater than 20% of the peak systolic longitudinal strain (2D speckle tracking) on the second echocardiography as compared to baseline.

    Time frame: Change between the echocardiography at baseline and the echocardiography 4 hours after.

07

Study locations

3 sites
  • Département d'anesthésie-réanimation Hôpital cardiologique Louis Pradel Groupe Hospitalier Est
    Bron, Bron 69500, France
  • Ruste Martin
    Bron, BRON 69500, France
  • Hopital Edourd Herriot
    Lyon, 69008, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05209230
Lead sponsor
Hospices Civils de Lyon
Responsible party
Sponsor
First posted
Jan 26, 2022
Start date
Apr 15, 2022
Primary completion
Dec 18, 2025
Completion
Dec 18, 2025
Last update
Jan 8, 2026

Study contacts

RUSTE Martin, MD, Msc
principal investigator · Hospices Civils de Lyon

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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