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Comparison of intravenous, local and oral Tranexamic Acid effect on reducing postoperative bleeding ?in coronary artery bypass graft surgery

Comparison of intravenous, local and oral Tranexamic Acid effect on reducing postoperative bleeding ?in coronary artery bypass graft surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141209020258N166
Enrollment
96
Registered
2021-10-03
Start date
2021-10-23
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

Coronary artery bypass graft surgery. Mechanical complication of coronary artery bypass graft and biological heart valve graft

Interventions

Intervention 1: Intervention group 1: One gram of Tranexamic Acid will be given orally (2 capsules of 500 mg with a glass of water). Intervention 2: Intervention group 2: 3 grams of Tranexamic Acid is

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All elective patients are candidates for coronary artery bypass graft surgery Lack of sensitivity to Tranexamic Acid

Exclusion criteria

Exclusion criteria: Death of patients Reluctance to participate in the study

Design outcomes

Primary

MeasureTime frame
Bleeding. Timepoint: Within 24 hours. Method of measurement: Observation.;Count of platelet received. Timepoint: Within 24 hours. Method of measurement: Count.;Number of fresh frozen plasma received. Timepoint: Within 24 hours. Method of measurement: Count.;Number of pack cell received. Timepoint: Within 24 hours. Method of measurement: Count.;Mortality. Timepoint: Within 72 hours. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Behnam Mahmodie

Arak University of Medical Sciences

mahmodie@arakmu.ac.ir+98 86 3222 2003

Outcome results

None listed

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