Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06535360
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-05-06
Brief Title:
Efficacy of Pathogen Inactivation Strategies for Platelet Transfusion
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Improving Efficacy and Safety of Pathogen Inactivation Strategies for Platelet Transfusion in Cardiac Surgical Patients on Cardiopulmonary Bypass
Status:
COMPLETED
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This is a prospective randomized clinical trial designed to determine the hemostatic ability of pathogen reduced platelet when compared to non-pathogen reduced platelets suspended in platelet additive solution
Detailed Description:
The safety and efficacy of pathogen reduced PRT platelets PLTs have been investigated in several controlled clinical studies Most of these clinical studies evaluated the efficacy of PRT PLTs during prophylactic transfusion evaluating post-transfusion platelet count increments rather than platelet function during bleeding episodes During massive transfusion events and immediate resuscitation PLT transfusion is recognized as an important determinant of a positive patient outcome PLT transfusion is important to control bleeding in patients undergoing cardiac surgery on cardiopulmonary bypass because cardiopulmonary bypass alters platelet function Thus transfusion of functional platelets is required to control bleeding post-operatively In this context the investigators propose to investigate whether efficient hemostasis associated with platelet transfusion differs with the use of pathogen reduced PRT PLTs compared to non-pathogen reduced PLTs that are suspended in platelet additive solution
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None