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Blood Conservation in Patients (3.5-12kg) Undergoing Congenital Cardiac Surgery

Congenital Heart Disease Clinical Trial

Official title:
Differences in Outcomes for Patients (3.5-12kg) Undergoing Congenital Cardiac Surgery Who Receive Blood Versus Those Who do Not

Clinical Trial Summary

To evaluate if there is any clinical difference in patients 3.5-12kg who undergo cardiac surgery with cardiopulmonary bypass that do and do not receive blood products as part of their procedure. The main hypothesis of the study is that the patients undergoing bloodless cardiac surgery will have decreased morbidity and mortality when compared to the cohort that did receive blood as well as a shorter ICU and hospital length of stay.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05881564
Study type Interventional
Source Augusta University
Contact
Status Recruiting
Phase N/A
Start date May 10, 2023
Completion date May 12, 2026
View Details
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