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Quantra Point-of-Care Hemostasis Monitoring — QUANTRA  

Bleeding Clinical Trial

Official title:
Quantra Point-of-Care Hemostasis Monitoring and Perioperative Blood and Blood Component Transfusion During High-Risk Complex Cardiac Surgery: A Randomized Clinical Trial

Clinical Trial Summary

The investigators will test the hypothesis that utilization of a blood and blood component transfusion algorithm guided by the POC Quantra QPlus System in patients undergoing complex cardiac surgery will reduce RBC, plasma, cryoprecipitate, and platelet transfusion during surgery and the first 12 postoperative hours, compared to standard of care (central laboratory transfusion monitoring at the primary anesthesia provider's discretion).

Clinical Trial Description

The Investigators propose a randomized control trial to assess patients scheduled for aortic surgery or high-risk cardiac surgery requiring cardiopulmonary bypass. Patients will be randomized 1:1 to routine care or POC Quantra QPlus System. The total number of blood and blood component transfusions (including RBC, plasma, cryoprecipitate, and platelets) during and after cardiac surgery until 12 hours after ICU arrival will be analyzed between the groups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06328647
Study type Interventional
Source The Cleveland Clinic
Contact Fabio Rodriguez, MD
Phone (216) 444-9950
Email rodrigf3@ccf.org
Status Not yet recruiting
Phase N/A
Start date July 1, 2024
Completion date December 31, 2026
View Details
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