drugset / Trial / NCT03014700

Fibrinogen Concentrate vs Cryoprecipitate

NCT03014700

Phase 4 Completed 60 enrolled Stanford University Emory University · collab
RandomizedParallel-groupSingle-blindTreatment

Summary

One of the most common hemostatic derangements in pediatric open- heart surgery is an acute acquired hypofibrinogenemia. This compromises fibrin clot generation and platelet aggregation, resulting in increased bleeding and allogenic blood transfusions. Currently, fresh frozen plasma and cryoprecipitate are used to supplement fibrinogen in pediatric cardiac patients. We propose that replacing cryoprecipitate with fibrinogen concentrate will be as effective in treating post-CPB bleeding and will decrease total blood product exposure when used as part of a blood transfusion algorithm. We plan to include all patients undergoing cardiac surgery on CPB less than 12 months and a fibrinogen level \<250mg/dL while on bypass. We hope to demonstrate that fibrinogen concentrate is at least as effective as the standard of care in the management of peri- operative bleeding in neonatal patients undergoing cardiopulmonary bypass. If we are able to demonstrate that fibrinogen is at least as effective as the standard of care, then we would plan a multi-center trial to demonstrate the safety and efficacy of this medication. If we are able to demonstrate that fibrinogen concentrate is effective, fibrinogen concentrate could replace allogenic products and potentially decrease transfusion related morbidity in mortality in this population.

Timeline

Start
2016-03
Primary completion
2018-04-25
Completion
2018-04-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cryoprecipitate Protein / enzyme biologic
Comparator Fibrinogen Concentrate Human Protein / enzyme biologic