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Multicenter Efficacy Study of Recombinant Human Erythropoietin in Acute Ischemic Stroke — ESS  

Stroke, Acute Clinical Trial

Official title:
German Multicenter EPO Stroke Trial (Phase II/III)

Clinical Trial Summary

The purpose of this randomized, double-blind, placebo-controlled multicenter study is to determine in a cohort of 506 patients with acute ischemic stroke in the middle cerebral artery territory, the effect of a three-day high-dose, intravenous erythropoietin treatment on functional outcome up to a follow-up of 90 days.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00604630
Study type Interventional
Source Max-Planck-Institute of Experimental Medicine
Contact
Status Completed
Phase Phase 2/Phase 3
Start date January 2003
Completion date June 2008
View Details
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