Overview

Renal Graft Function After Treatment With Erythropoietin (EPO)

Status:
Terminated
Trial end date:
2013-03-01
Target enrollment:
0
Participant gender:
All
Summary
Background : Numerous studies have outlined the cellular pleiotropic effects of erythropoietin (EPO) and their role in the prevention of ischemic-reperfusion lesion such as after acute ischemic injury of the brain or the heart. However, most of these studies were carried out in animal models and no definitive proof exists today to demonstrate that EPO has similar beneficial effects in human pathology. Purpose : The aim of the study is to demonstrate that in humans, EPO can protect against ischemic-reperfusion lesions in a model of ischemia i.e. kidney transplantation.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Hospital, Limoges
Collaborator:
Hoffmann-La Roche
Treatments:
Epoetin Alfa
Criteria
Inclusion Criteria:

- donor:

- cadaveric organ donor,

- age ≥ 18 years,

- mono-organ (kidney) retrieval,

- retrieval done in the centres of Limoges, Bordeaux, Toulouse, Angers, Brest,
Nantes, Poitiers, Rennes, Tours,

- hematocrit ≤ 45%.

- Recipient:

- age ≥ 18 years,

- on the waiting list for a kidney graft.

Exclusion Criteria:

- living donors,

- age under 18 years,

- multi-organ retrieval,

- donor hematocrit above 45%