The Effect of Human Recombinant Erythropoietin in Acute Renal Failure
Completed · Phase 2
Conditions studied: Acute Kidney Injury
In brief
The purpose of this study is to determine if the use of erythropoietin when used in high dose during acute kidney injury can decrease the number of days of kidney injury.
Key facts
- Study ID
- NCT03102021
- Run by
- North Texas Veterans Healthcare System
- People needed
- 25
- Starts
- 2006-03-01
- Expected to finish
- 2013-06-01
- Last updated by the study team
- 2017-04-05
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- age equal or greater than 21 yo
- acute neprhotoxic or ischemic kidney injury, acute tubular necrosis
You may not qualify if…
- no active or current malignancies
- not actively receiveing epo
- GFR less than 60 ml/min
- unable to provide informed consent
- contraindication to erythropoietin use
Where it is running
- Dallas VAMC — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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