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Phase 4 N=60 Randomized Single-blind Treatment

Fibrinogen Concentrate vs Cryoprecipitate

Congenital Heart Disease

Enrolled (actual)
60
Serious AEs
10.0%
Results posted
May 2019
Primary outcome: Primary: Total Units of Intraoperative Allogenic Donor Transfusions (ADT) Administered During Procedure Through ICU Arrival. — 5; 4 ADT units

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Fibrinogen Concentrate (Biological); Cryoprecipitate (Biological)
Age
Pediatric · 0+ yrs
Sex
All
Sponsor
Stanford University
Primary completion
Apr 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Total Units of Intraoperative Allogenic Donor Transfusions (ADT) Administered During Procedure Through ICU Arrival.
5; 4
SECONDARY
Chest Tube Output
18.05; 16.11
SECONDARY
Hours of Mechanical Ventilation
30.32; 27.10
SECONDARY
Length of Stay in Intensive Care Unit (ICU)
4.50; 3.00
SECONDARY
Length of Stay in Hospital
8.00; 7.00
SECONDARY
Count of Participants Who Died Within 30 Days Following Procedure
0; 1

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.

Eligibility Criteria

Inclusion Criteria

  • Neonates of at least 32 weeks of gestational age and infants up to 12 months of age with the diagnosis of congenital heart disease, requiring open heart surgery with cardiopulmonary bypass

Exclusion Criteria

  • Pre-existing coagulopathy, including unexplained bleeding or history of clotting
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03014700). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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