Is Myocardial Stunning Induced by Continuous Renal Replacement Therapy a Reality in Critically Ill Patients?
NCT ID: NCT05209230
Last Updated: 2026-01-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
42 participants
INTERVENTIONAL
2022-04-15
2025-12-18
Brief Summary
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The investigator hypothesize that myocardial stunning induced by renal replacement therapy is frequent, independent from cardiac loading conditions and associated with peripheral hypoperfusion.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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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
Continuous renal replacement therapy
Continuous renal replacement therapy (veno venous hemofiltration) without net ultrafiltration, through a dedicated central venous catheter
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.
Control group
Continuous renal replacement therapy is differed from 6 hours to allowed 2 control echocardiographic evaluations
Interventions
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Continuous renal replacement therapy
Continuous renal replacement therapy (veno venous hemofiltration) without net ultrafiltration, through a dedicated central venous catheter
Control group
Continuous renal replacement therapy is differed from 6 hours to allowed 2 control echocardiographic evaluations
Eligibility Criteria
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Inclusion Criteria
* Acute Kidney Injury grade 3 (KDIGO)
* Indication for renal replacement therapy for the clinician in charge
Exclusion Criteria
* Poor echogenicity with speckle tracking analysis failure
* Chronic hemodialysis
* Extra corporeal membrane oxygenation, left ventricular assist device.
18 Years
90 Years
ALL
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Principal Investigators
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RUSTE Martin, MD, Msc
Role: PRINCIPAL_INVESTIGATOR
Hospices Civils de Lyon
Locations
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Département d'anesthésie-réanimation Hôpital cardiologique Louis Pradel Groupe Hospitalier Est
Bron, Bron, France
Ruste Martin
Bron, BRON, France
Hopital Edourd Herriot
Lyon, , France
Countries
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Other Identifiers
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69HCL21_1013
Identifier Type: -
Identifier Source: org_study_id
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