ClinicalTrials.Veeva

Menu

Effect of Preoperative Recombinant Human Erythropoietin on Transfusion Risk in Valvular Heart Surgery

Yonsei University logo

Yonsei University

Status

Completed

Conditions

Cardiac Surgery

Treatments

Drug: rhEPO

Study type

Interventional

Funder types

Other

Identifiers

NCT00939978
4-2008-0427

Details and patient eligibility

About

The administration of rhEPO on the one day before cardiac surgery will be effective to decrease the bleeding due to the surgery.

Enrollment

74 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The 90 patients who are planned to have the heart surgery during this study period.(minimum age 20)

Exclusion criteria

  • Uncontrolled hypertension(diastolic blood pressure(DBP)>100 mmHg), Hct > 45%, Plt. count)>450,000
  • There are no history of seizure, thrombus, cancer, acute hepatitis, alcoholism, peripheral blood vessel disease, pure red blood cell dysfunction, liver function failure, chronic multiple arthritis.
  • No pregnancy, acute hyper parathyroidism.

Trial design

74 participants in 2 patient groups, including a placebo group

Venoferrum
Active Comparator group
Treatment:
Drug: rhEPO
saline
Placebo Comparator group
Treatment:
Drug: rhEPO

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems