Autologous Cold-stored Apheresis Platelets
NCT07064954 · Status: NOT_YET_RECRUITING · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 100
Last updated 2025-07-22
Summary
The Auto-PLTS Study is a single-centre trial performed at Toronto General Hospital (TGH) that uses a randomized, patient preference design. The recent introduction of cold-stored platelets with a shelf-life of 14 days into clinical practice has made it possible to offer autologous apheresis platelet predonation to patients undergoing elective cardiac (and other high-blood-loss) surgeries while allowing sufficient time to recover platelet count before surgery. The Auto-PLTS Study is designed to assess whether replacing allogeneic platelets with autologous platelets will improve patient outcomes and benefit the healthcare system by reducing the burden on allogeneic platelet supply. The study is also designed to determine whether patients are willing to donate autologous platelets 7-10 days prior to surgery.
Conditions
- Bleeding
- Platelets
- Cardiopulmonary Bypass
- Cardiac Surgery
Interventions
- BIOLOGICAL
-
Autologous Cold-Stored Platelets
Two units of autologous platelets will be collected via an apheresis machine that draws blood from an intravenous (IV) line over 1-2 hours, isolates and leukoreduces the platelets by centrifugation and returns the remaining blood back to the patients. Collected autologous platelets will be stored at 1-6℃ without agitation until they are needed during or after surgery or 14 days have elapsed since their collection, after which they will be destroyed as per standard institutional procedures for expired blood products. For the first two platelet orders within 24 hours of cardiopulmonary bypass (CPB) termination, patients will receive their autologous cold-stored platelets. For the third and subsequent doses, patients in the intervention group will receive allogeneic room temperature-stored platelets (standard of care).
- BIOLOGICAL
-
Allogeneic Room Temperature-Stored Platelets (Standard of Care)
Allogeneic platelets will be collected by Canadian Blood Services as per their standard operating procedures. Room temperature stored platelets will be stored at 20-24°C with constant agitation for up to 7 days as per current practices. For any platelet orders within 24 hours of cardiopulmonary bypass (CPB) termination, patients in the control group will receive allogeneic platelets as per usual care.
Sponsors & Collaborators
-
University Health Network, Toronto
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-09-01
- Primary Completion
- 2026-12-31
- Completion
- 2027-04-30
Countries
- Canada
Study Locations
More Related Trials
-
Platelet Function After Cardiac Surgery.
NCT06405516 ·Status: RECRUITING ·Phase: NA
-
Association Between Perioperative Platelet Function and Major Adverse Perioperative Events
NCT00901030 ·Status: COMPLETED
-
The Cryopreserved vs. Liquid Platelets Trial
NCT03991481 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Cold Stored Whole Blood in Cardiothoracic Surgery
NCT04988620 ·Status: RECRUITING ·Phase: NA
-
Cold Apheresis Platelets in PAS
NCT02754414 ·Status: UNKNOWN ·Phase: PHASE1
-
Factor Replacement in Surgery
NCT04114643 ·Status: UNKNOWN ·Phase: PHASE2
-
PLATelet Function Operating Room Monitoring
NCT03121898 ·Status: COMPLETED
-
CHIlled Platelet Study "CHIPS"
NCT04834414 ·Status: COMPLETED ·Phase: PHASE3
-
Platelet Inhibition and Bleeding in Patients Undergoing Emergent Cardiac Surgery
NCT01468597 ·Status: COMPLETED
-
Platelet Inhibition and Bleeding in Patients Undergoing Non-Cardiac Surgery
NCT01606865 ·Status: COMPLETED
-
COmbined pLaTelet and eRythrocyte AutotransfusioN During Cardiac surgEry (COLTRANE) Trial
NCT06425614 ·Status: RECRUITING ·Phase: NA
-
Intraoperative Cell Saver Autotransfusion Use for Major Surgical Oncology Operations.
NCT00708513 ·Status: COMPLETED
-
Thromboelastography (TEG®) and Platelet Function in Patients on Anti-platelet Agents
NCT00901160 ·Status: TERMINATED
-
STUDY OF SURVIVAL AND FUNCTIONALITY IN CRYOPRESERVED PLATELETS
NCT04754841 ·Status: UNKNOWN ·Phase: NA
-
Platelet and Autotransfusion Device in Cardiac Surgery
NCT06629311 ·Status: RECRUITING
-
Correlation Between Reticulated Platelets and Major Adverse Cardiac and Cerebrovascular Events After Noncardiac Surgery
NCT02097602 ·Status: COMPLETED
-
Transfusion of Plasma Prior to Invasive Procedures Pilot Trial (TOPPIT)
NCT02561026 ·Status: UNKNOWN ·Phase: PHASE3
-
Occurrence of Bleeding and Thrombosis During Antiplatelet Therapy in Non-cardiac Surgery
NCT01358422 ·Status: COMPLETED
-
Advance Targeted Transfusion in Anemic Cardiac Surgical Patients for Kidney Protection: A Proof of Concept Pilot Study
NCT00861822 ·Status: COMPLETED ·Phase: PHASE1
-
Active Preoperative Anemia Management in Patients Undergoing Cardiac Surgery
NCT02189889 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
Comparison of the Performance and Effectiveness of Two Transfusion-Saving Devices: Cell-Saver and SAME
NCT06766032 ·Status: COMPLETED
-
Use of PRP in Open Surgery for Type A Aortic Dissection
NCT07005661 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2/PHASE3
-
Assessing the Hemostatic Efficacy of Pathogen Reduced Platelets in Children Undergoing Cardiopulmonary Bypass Surgery: A Pilot Clinical Trial
NCT05293106 ·Status: TERMINATED ·Phase: PHASE4
-
Evaluating URMC's Massive Transfusion Protocol
NCT02083549 ·Status: COMPLETED
-
In Vivo Study to Assess the Recovery and Survival of Radiolabeled Autologous INTERCEPT Apheresis Platelet Components Suspended in 100% Plasma Stored for up to 7 Days
NCT04022889 ·Status: COMPLETED ·Phase: PHASE2