Loading clinical trials...
Loading clinical trials...
Coagulopathic-induced bleeding after cardiopulmonary bypass in cardiac surgery patients is common and is associated with adverse outcomes in cardiac surgery. The hypothesis of the study is that FEIBA will be a more effective treatment than standard of care (FFP) in cardiac surgery patients who have coagulopathic-induced bleeding. This study is being conducted to determine the efficacy of FEIBA versus FFP as first line therapy in correcting coagulopathic induced microvascular bleeding in cardiac surgery patients.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
North Shore University Hospital
Manhasset, New York, United States
Start Date
November 3, 2025
Primary Completion Date
November 1, 2028
Completion Date
November 1, 2029
Last Updated
March 11, 2026
140
ESTIMATED participants
FEIBA
DRUG
FFP
DRUG
Lead Sponsor
Northwell Health
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04246463