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Cardiac MRI for the Detection of Myocardial Injury Following Acute Kidney Injury

Multiparametric Cardiac MRI for the Detection and Quantification of Myocardial Injury Following Acute Kidney Injury (Cardiorenal Syndrome Type 3)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05034588
Enrollment
40
Registered
2021-09-05
Start date
2021-04-07
Completion date
2023-12-31
Last updated
2021-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury, Cardio-Renal Syndrome, Cardiomyopathies

Keywords

Cardiac MRI

Brief summary

The aim of this clinical prospective study is to assess structural and functional myocardial changes in patients after acute kidney injury (Cardiorenal syndrome type 3) and intensive care stay by multiparametric cardiac MRI.

Detailed description

The aim of the study is to demonstrate any differences in myocardial structure and function using multiparametric cardiac MRI in patients after acute kidney injury (Cardiorenal syndrome type 3) and intensive care stay and subsequent convalescence compared to a control group with intensive care stay but without kidney injury. Furthermore, the correlation between clinical disease severity and cardiac involvement will be investigated.

Interventions

Multiparametric cardiac magnetic resonance, including functional and structural parameter

Sponsors

University Hospital, Bonn
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years

Inclusion criteria

1. acute kidney injury and convalescence (GFR \> 45 ml/min/1.73m²). 2. patients who are 18 years of age or older

Exclusion criteria

1. underlying cardiac disease, e.g. known myocardial infarction, previous myocarditis, congenital heart disease, cardiomyopathies of other causes 2. known underlying disease wit potential cardiac involvement, e.g. storage disease (e.g. hemochromatosis, Fabry disease), inflammatory (e.g. sarcoidosis), endocrinological (e.g. diabetes mellitus, hyper-/hypothyroidism), autoimmune (e.g. systemic lupus erythematosus, dermatomyositis, rheumatoid arthritis), therapeutic (chemotherapy). 3. patients with persistent renal failure and GFR \< 45 ml/min/1.73m² 4. allergy to contrast media 5. patients who are using a intrauterinpessare for contraception 6. pregnant and breastfeeding women 7. patients with contraindications for MRI due to implants

Design outcomes

Primary

MeasureTime frameDescription
Myocardial T1 relaxation timeMeasurement will be performed within 2 weeks after MRI scan.T1 relaxation times will be obtained to asses acute myocardial injury and fibrosis. T1 maps will be analyzed using a segmental approach by region of interest analysis. T1 relaxation times are given in \[ms\].

Secondary

MeasureTime frameDescription
Myocardial T2 relaxation timeMeasurement will be performed within 2 weeks after MRI scan.T2 relaxation times will be obtained to asses myocardial edema. T2 maps will be analyzed using a segmental approach by region of interest analysis. T2 relaxation times are given in \[ms\].
Myocardial ECVMeasurement will be performed within 2 weeks after MRI scan.Myocardial extracellular volume will be obtained to asses extracellular space/myocardial fibrosis. ECV values will be calculated using a segmental approach by region of interest analysis of native and contrast-enhanced T1 relaxation maps. ECV values are given in \[%\].
Myocardial strainMeasurement will be performed within 2 weeks after MRI scan.Cardiac magnetic resonance feature-tracking will be used to asses left ventricular longitudinal, circumferential and radial strain.

Countries

Germany

Contacts

Primary ContactJulian A Luetkens, PD Dr. med.
julian.luetkens@ukbonn.de+49 228 287-15960
Backup ContactAlexander Isaak, PD Dr. med.
alexander.isaak@ukbonn.de+49 228 287-15960

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026