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The effect of erythropoietin in reduction of tissue–reperfusion injury after coronary artery baypass graft

The effect of erythropoietin in reduction of tissue–reperfusion injury after coronary artery baypass graft

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138809102799N1
Enrollment
50
Registered
2010-01-25
Start date
2009-12-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Tissue-reperfusiuon injury. Atherosclerotic heart disease

Interventions

Intervention 1: Erythropoietin (660 U/kg, 5 minutes after the end of cross clamp). Intervention 2: no intervention in control group.
Treatment - Drugs
Erythropoietin (660 U/kg, 5 minutes after the end of cross clamp)
no intervention in control group

Sponsors

Deputy of Research and Technology of Mazandarn University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: sign of angina pectoris need to revascularization after angiography, presence of indication for CABG Exclusion criteria: history of Myocardial Infarction since 3 months prior to the study, EF16 , Cr > 2.5, receiving Erythropoietin since 6 months prior to the study, blood pressure > 150/95, history of Arterial fibrillation blood transfusion since 3 months prior to the study, heavy or cardiac trauma since 3 months prior to the study, polycytemia vera

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Cardiac marker (CKMB). Timepoint: Before and 10 hours after surgery. Method of measurement: labratory.;Cardiac marker (Troponin I). Timepoint: Before and 10 hours after surgery. Method of measurement: labratory.

Primary

MeasureTime frame
Cardiac function (Wall Motion Score Index). Timepoint: 4 days, 30 days. Method of measurement: echocardiography.;Cardiac function (Ejection Fraction). Timepoint: Before surgery, 4 days and 30 days after surgery. Method of measurement: echocardiography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShervin Ziabakhsh Tabary

Mazandaran University of Medical Sciences

Sziabakhsh@mazums.ac.ir+98 912 354 6414

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026