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Evaluation of AKI by Measuring the NephroCheck Test After Pediatric Cardiac Surgery

Evaluation of the Incidence of Renal Stress by Measuring the NephroCheck Test After Pediatric Cardiac Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03963284
Enrollment
350
Registered
2019-05-24
Start date
2019-06-30
Completion date
2020-06-30
Last updated
2019-05-24

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

Conditions

Acute Kidney Injury, Cardiac Disease, Surgery

Brief summary

Blood and urine samples of over 200 pediatric subjects (over 28 days to 3 years) undergoing complex cardiac surgery with cardiopulmonary bypass (CPB) will be collected at several time points to measure corresponding biomarkers such as serum creatinine, serum urea concentration, or NephroCheck test (\[TIMP-2\]\*\[IGFBP7) to evaluate the diagnostic performance of AKI by NephroCheck test .

Detailed description

At least 200 subjects having undergone pediatric cardiac surgery with cardiopulmonary bypass (CPB). Enrollment will continue with a maximum of 350 subjects until 30 cases of AKI (stage 2 and 3) are reached. Blood and urines samples will be collected at several time points to measure biomarkers and set up a biobank. The samples used within the scope of this protocol will be fresh urine samples (1 to 2 ml) and blood samples. Urine samples for \[TIMP-2\]\*\[IGFBP7\] measurements will be taken from each subject included in the study during the first 48 hours following cardiopulmonary bypass initiation according to the following schedule: * baseline before initiation of cardiopulmonary bypass (CPB, 0h). * \- 2h, 4h, 6h, 8h, 12h, 24h, 48h after initiation of CPB Blood samples for serum creatinine and urea concentration measurement will be taken from each subject included in the study during the first 48 hours following cardiopulmonary bypass initiation according to the following schedule: * baseline before initiation of cardiopulmonary bypass (CPB, 0h). * 12h, 24h, 48h, 60h after initiation of CPB Primary objective: To evaluate the proportion of subjects predicted to be at risk of AKI (stage 2 and 3) using at least one measurement of NephroCheck in subjects having undergone pediatric cardiac surgery. Secondary objectives: * To evaluate the incidence of AKI (stage 2 and 3) according to the KDIGO guideline * To study the kinetic profile of cell cycle arrest biomarkers (TIMP-2\*IGFBP-7) during the first 48 hours in subjects having undergone pediatric cardiac surgery * To determine the baseline values of \[TIMP-2\]\*\[IGFBP7\] in the targeted population before surgery * To determine profile differences of \[TIMP-2\]\*\[IGFBP7\] between AKI (stage 2 and 3) and non-AKI groups * To evaluate the diagnostic performances of \[TIMP-2\]\*\[IGFBP7\] to predict AKI after pediatric cardiac surgery using a cut-off value of 0.3

Interventions

PROCEDUREcardiac surgery

pediatric cardiac surgery with cardiopulmonary bypass

Urine of the subjects undergoing cardiac surgery with CPB will be tested by NephroCheck test

Sponsors

BioMérieux
CollaboratorINDUSTRY
Shanghai Children's Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
28 Days to 3 Years
Healthy volunteers
No

Inclusion criteria

* Must sign the consent form * Clinical diagnosis of complex congenital heart surgery (Risk Adjusted classification for Congenital Heart Surgery \[RACHS\] score \>=2) * Must undergo elective cardiac surgery with CPB

Exclusion criteria

* Clinical diagnosis of severe pre-existing renal insufficiency (SCr \>2 times age-adjusted normal range) * Significant abnormalities of the kidneys or genitourinary tract

Design outcomes

Primary

MeasureTime frameDescription
Test fresh urine samples by NephroCheckup to one yearUrine samples for \[TIMP-2\]\*\[IGFBP7\] measurements will be taken from each subject included in the study during the first 48 hours following cardiopulmonary bypass initiation according to the following schedule: * baseline before initiation of cardiopulmonary bypass (CPB, 0h). * \- 2 hours, 4 hours, 6 hours, 8 hours, 12 hours, 24 hours, 48 hours after initiation of CPB

Secondary

MeasureTime frameDescription
Test serum creatinine and urea concentration to report AKI according KDIGO guidelineup to one yearBlood samples for serum creatinine and urea concentration measurement will be taken from each subject included in the study during the first 48 hours following cardiopulmonary bypass initiation according to the following schedule: * baseline before initiation of cardiopulmonary bypass (CPB, 0 hours). * 12 hours, 24 hours, 48 hours, 60 hours after initiation of CPB

Contacts

Primary ContactXi Mo, Doctor
moxi@scmc.com.cn8618930830620

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026