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Effects of Recombinant Human Erythropoietin on Platelet Function in Healthy Subjects

Effects of Recombinant Human Erythropoietin on Platelet Function in Healthy Subjects

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00368238
Enrollment
96
Registered
2006-08-24
Start date
2005-10-31
Completion date
2006-07-31
Last updated
2006-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Subjects

Keywords

Platelet function tests, Erythropoietin, Aspirin, Clopidogrel

Brief summary

The purpose of this study is to see if a naturally-occurring hormone called erythropoietin changes the action of platelets in the blood. Erythropoietin is made by the kidneys to stimulate red blood cell production to prevent anemia. Platelets are small cells in the blood that help clot blood in case of injury. Platelets also sometimes form blood clots in blood vessels that may cause heart attacks. This study is trying to determine whether erythropoietin increases the clotting action of platelets. Information on erythropoietin in healthy subjects may eventually help in the treatment of patients with heart attacks.

Detailed description

Anti-apoptotic effects of erythropoietin in experimental myocardial infarction and ischemia-reperfusion injury suggest potential for therapeutic benefit in patients with acute MI. Before the therapeutic potential of rHuEpo in acute MI can be tested in large clinical trials, more information on the effects of short-term rHuEpo on platelet function are needed. Accordingly, the current proposal aims to determine the effects of 3 doses of rHuEpo (100U/kg, 200U/kg and 400U/kg daily for 3 days) on platelet function and other safety measures in healthy subjects. Specific Aim: To determine the effects of three ascending doses of rHuEpo vs. placebo on in vivo and in vitro platelet function in healthy subjects treated with aspirin and clopidogrel. Hypotheses to be tested: 1) 1) Short-term administration of rHuEpo does not alter bleeding time responses to aspirin and clopidogrel when compared with placebo. 2) Short-term administration does not alter in vitro platelet aggregation responses to aspirin and clopidogrel when compared with placebo.

Interventions

DRUGAspirin (drug)
DRUGClopidogrel (drug)

Sponsors

American Heart Association
CollaboratorOTHER
Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
21 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 21-40 years * Able and willing to provide written informed consent * Bleeding time \<10 minutes

Exclusion criteria

* Any chronic medical disease * Chronic or frequent over-the-counter or prescription medication use * Hemoglobin \>15 gm/dl for both genders or \<13 gm/dl (men) or \<12 gm/dl (women) * Platelet count \>400,000/µl or \<150,000/µl * Blood pressure \> 140/90 mmHg

Design outcomes

Primary

MeasureTime frame
Bleeding time
Platelet function assay closure time

Secondary

MeasureTime frame
PTT
Complete Blood Count
von Willebrand factor
P-selectin
PT

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026