RecruitingNot ApplicableNCT06493227

Extended Perioperative Administration of Fibrinolysis Inhibitors After Cardiac Surgery

The Practice of Routine Extended Perioperative Administration of Fibrinolysis Inhibitors to Reduce the Risk of Bleeding in Cardiac Surgery. Multicenter Prospective Randomized Cluster Crossover Study


Sponsor

Saint Petersburg State University, Russia

Enrollment

1,373 participants

Start Date

Aug 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

PRIORITY is a pragmatic, multi-center, cluster crossover trial that aims to evaluate whether implementing a policy of routine extended (intraoperative and 4 hour after transfer to ICU) use of fibrinolysis inhibitors leads to a decrease in post-operative blood transfusion compared to a policy that only involves intraoperative use.


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • A hospital that performs a minimum of 250 open heart interventions per year.
  • Consent from hospital physicians regarding the prophylactic use of fibrinolysis inhibitors (more than 95% of physicians involved in the treatment of adult patients (>18 years) agree to adhere to the strategy of using fibrinolysis inhibitors as prescribed by the study protocol).

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERNo routine fibrinolysis inhibitors after surgery

Tranexamic acid or epsilon-aminocaproic acid should be administered intravenously during surgery. The dosage and method of administration should be followed according to the routine practice of the participating site.

OTHERRoutine fibrinolysis inhibitors after surgery

During surgery, it is recommended to administer 70% of the routine dose of Tranexamic acid or epsilon-aminocaproic acid intravenously. Following the surgery, the remaining 30% of this dose should be administered as a continuous intravenous infusion over the course of the first 4 hours.


Locations(2)

Cardiac surgery department, Saint-Petersburg state university hospital

Saint Petersburg, Russia

St. Petersburg State University Hospital

Saint Petersburg, Russia

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06493227


Related Trials