Trials / Unknown
UnknownNCT01066351
Efficacy of Erythropoietin to Prevent Acute Kidney Injury in Chronic Kidney Disease Patients Undergoing Cardiac Surgery
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- Sponsor
- Thammasat University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to demonstrate the efficacy of erythropoietin for prevention acute kidney injury in CKD patients undergoing cardiac surgery.
Detailed description
Acute kidney injury (AKI)occur 7.7-42% after cardiac surgery. The incidence of AKI requiring renal replacement therapy following coronary artery bypass grafting (CABG) surgery was 0.7-3.5% and increase mortality rate. Erythropoietin (EPO) is now considered a novel anti-apoptotic and anti-inflammatory action. The present study was designed to evaluate the administration of EPO as a means of preventing AKI in these patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | beta erythropoietin | The patients were assigned to receive beta erythropoietin (Recormon) dose 200 unit/kg at 3 day before cardiac surgery and 100 unit/kg in the morning before cardiac surgery. |
| DRUG | placebo | The patients were assigned to receive normal saline same volume at 3 day before cardiac surgery and in the morning before cardiac surgery. |
Timeline
- Start date
- 2010-01-01
- Primary completion
- 2011-03-01
- Completion
- 2011-06-01
- First posted
- 2010-02-10
- Last updated
- 2010-02-10
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT01066351. Inclusion in this directory is not an endorsement.