CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 44 enrolled
Drug / intervention
Recombinant human erythropoietin alfa (drug) +1 moredrug
Likely dose
Recombinant human erythropoietin alfa 200 U/kg IV daily for 3 daysAI-extracted
Key inclusion· 4
  • Age 21 to 75 years
  • Acute myocardial infarction with total or sub-total coronary occlusion documented on angiography
  • Successful percutaneous revascularization with restoration of TIMI grade 3 coronary flow
  • Current treatment with aspirin and a thienopyridine (clopidogrel or ticlopidine)
Key exclusion· 4
  • Hemodynamic instability, cardiogenic shock, or severe congestive heart failure
  • Time from symptom onset to revascularization procedure exceeding 16 hours
  • Prior treatment with intravenous thrombolytic agents for acute myocardial infarction
  • Anticipated need for additional revascularization procedures

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00367991
NCT00367991Phase 2Completed

Effects of Recombinant Human Erythropoietin on Platelet Function in Patients With Acute Myocardial Infarction

Yale University·interventional·Posted Aug 24, 2006·Updated Jan 12, 2018

In Brief

A Phase 2 clinical trial evaluating Recombinant human erythropoietin alfa (drug) and Placebo for Myocardial Infarction. Completed, enrolled 44 participants across 1 site.

Detailed Summary

The purpose of this study is to see if a naturally-occurring hormone called erythropoietin changes the action of platelets in the blood. Patients with heart attacks are treated with medicines to reduce the clotting action of platelets. This study is trying to determine whether erythropoietin alters the clotting action of platelets in patients receiving anti-platelet medicines. It is important to understand the effects of erythropoietin on platelets since preliminary studies in animals suggest that erythropoietin may protect the heart from damage during a heart attack.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedAug 24, 2006
Enrollment StartNov 1, 2006
Primary CompletionMar 1, 2008
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 19.9 years ago

Interventions

Recombinant human erythropoietin alfa (drug)drug

200 U/kg IV daily for 3 days vs. matched volume of normal saline IV daily for 3 days

Placebodrug

Normal saline to match active drug (rHuEpo)