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Transfusion Reaction clinical trials

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NCT ID: NCT04388722 Withdrawn - Hypovolemia Clinical Trials

Monitoring Noninvasively for Infusion and Transfusion Optimization

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

This is a multicenter, cluster randomized controlled trial to assess the effects of an optimized intraoperative fluid and blood management strategy on postoperative complications.

NCT ID: NCT03444610 Withdrawn - Clinical trials for Blood Transfusion Complication

Can we Transfuse Blood Over Shorter Period ?

Start date: May 31, 2018
Phase: Phase 1
Study type: Interventional

Blood transfusion is very lengthy procedure and consumes a substantial time from patients and health care providers. On average, it may take most if not all the working day which leads to significant constrains on hospital bed utilization. It starts from pre-transfusion testing, clinical assessment, actual administration of blood and post-transfusion care. The main bulk of this procedure is usually related to administration of the blood which typically given over 3 hours (5ml/kg/hour), although there is no strong evidence to support that. Indeed, it has been accepted as standard of care to transfuse blood over short time as in emergency situations. OBJECTIVE: To determine the maximum tolerated blood transfusion rate that can be safely delivered in patient who required blood transfusion i.e. transfusing blood over short time. METHOD: This is a phase I, open label, nonrandomized, prospective and rate-finding study. A well-known dose escalation design called 3+3 design will be used to identify the maximum tolerated rate. To assure the safety of such procedure, blood transfusion rate will be escalated very slowly by 1 ml/kg/hour for each cohort until rate-limiting toxicities or maximum of 10ml/kg/hour.

NCT ID: NCT03056378 Withdrawn - Anemia Clinical Trials

POOLED Red Blood Cells Prepared From Pooling 5 Leukoreduced, Irradiated RBC Units

Pooled RBCs
Start date: October 2019
Phase: Phase 1
Study type: Interventional

The purpose of the study is to determine the safety of pooled red blood cells (RBCs) compared to standard leukoreduced RBC products stored in additive solution. The primary objective is to determine if there is no significant difference in transfusion associated adverse events in POOLED-RBCs compared to standard RBC product groups. Secondarily to determine if there are no significant differences in new antibody and new positive direct antiglobulin test (DAT) formation in the POOLED-RBCs compared to standard RBC product groups.

NCT ID: NCT01463345 Withdrawn - Clinical trials for Post Cardiac Surgery

Blood Conservation in Cardiac Surgery

Start date: November 2011
Phase: N/A
Study type: Interventional

The objective of the study is to examine the safety of two different hemoglobin (Hgb)-based transfusion triggers in patients post cardiac surgery.