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Evaluating Erythropoietin as an Indicator for Possible Kidney Injury After Cardiac Surgery

EPO: A Renal Biomarker After Cardiac Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01393418
Acronym
EPO
Enrollment
80
Registered
2011-07-13
Start date
2010-11-30
Completion date
2012-03-31
Last updated
2016-12-15

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

Conditions

Acute Kidney Injury, Erythropoietin, Renal Biomarker

Keywords

Erythropoietin, Cardiac Surgery, Renal Biomarker, Acute Kidney Injury, Hypothermic Circulatory Arrest

Brief summary

The purpose of the study is to evaluate kidney biomarkers and determine if there is a correlation between Erythropoietin (EPO) levels and acute kidney injury after cardiac surgery. An early biomarker for kidney injury may be helpful in identifying, monitoring and managing patients at risk for kidney failure after cardiac surgery. To evaluate Erythropoietin's role as a predictor of poor renal function in the immediate post-bypass period we plan to compare EPO levels to Neutrophil gelatinase-associated lipocalin (NGAL).

Detailed description

Acute kidney injury (AKI) is a serious complication after cardiac surgery and cardio-pulmonary bypass. AKI is associated with high mortality. Erythropoietin, a hormone produced by the kidneys, will be evaluated as a potential biomarker of kidney injury. Neutrophil gelatinase-associated lipocalin (NGAL) has been studied as a biomarker of kidney injury. Early kidney injury detection has been long sought and NGAL has been shown to be a promising biomarker. A troponinlike biomarker of AKI that is easily measured and capable of both early detection and risk stratification would represent an advancement in our ability to differentiate acute kidney injury from failure. Investigating EPO as a biomarker may prove to have increased predictive value in the clinical care of cardiac surgery patients.

Interventions

OTHERCardiac Surgery

Sponsors

University of Michigan
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Cardiac surgery with cardiopulmonary bypass with DHCA * Normal renal function or renal insufficiency-serum creatinine less than 2.5 mg/dL * Adult male and female patients 18 years and older

Exclusion criteria

* VADS * Emergent cases * Prolonged hypoxemia before, during or after bypass * End stage renal disease * Patients receive erythropoietin receptor agonists

Design outcomes

Primary

MeasureTime frame
Renal injury/Failure18 Hours after surgery

Countries

United States

Outcome results

None listed

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