Evaluating Erythropoietin as an Indicator for Possible Kidney Injury After Cardiac Surgery
Completed
Conditions studied: Erythropoietin, Acute Kidney Injury, Renal Biomarker
In brief
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).
Key facts
- Study ID
- NCT01393418
- Run by
- University of Michigan
- People needed
- 80
- Starts
- 2010-11-01
- Expected to finish
- 2012-03-01
- Last updated by the study team
- 2016-12-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- VADS
- Emergent cases
- Prolonged hypoxemia before, during or after bypass
- End stage renal disease
- Patients receive erythropoietin receptor agonists
Where it is running
- University of Michigan Hospital — Ann Arbor, Michigan, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.