CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 60 enrolled
Drug / intervention
Fibrinogen Concentrate +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03014700
NCT03014700Phase 4Completed

Repurposing of Fibrinogen Concentrate as a Cost-Effective and Safe Hemostatic Agent in Infants Undergoing Cardiac Surgery on Cardiopulmonary Bypass

Stanford University·interventional·Posted Jan 9, 2017·Updated May 7, 2019

In Brief

A Phase 4 clinical trial evaluating Fibrinogen Concentrate and Cryoprecipitate for Congenital Heart Disease. Completed, enrolled 60 participants across 2 sites.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsEmory University

Timeline

Phase 4CompletedFinished
20162017201820192020202120222023202420252026
First PostedJan 9, 2017
Enrollment StartMar 1, 2016
Primary CompletionApr 25, 2018
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 9.5 years ago

Interventions

Fibrinogen Concentratebiological

Subject will be administered Fibrinogen Concentrate to control bleeding after open heart surgery when randomized to Fibrinogen Concentrate group

Cryoprecipitatebiological

Subject will be administered Cryoprecipitate to control bleeding after open heart surgery when randomized to Cryoprecipitate group