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Transfusion clinical trials

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NCT ID: NCT05661838 Completed - Spinal Fusion Clinical Trials

Effect of Intraoperative Allogeneic Blood Transfusion on Postoperative Pulmonary Complications

Start date: August 1, 2013
Phase:
Study type: Observational

Elective spine surgery is associated with a high incidence of perioperative complications, including peri- and postoperative pulmonary complications (PPCs), which occur in nearly 4% of patients. More than 40% of all deaths after elective spine surgery are attributed to PPCs. However, whether it influences risk of other PPCs is unclear.

NCT ID: NCT05452538 Completed - Hemorrhage Clinical Trials

AutoTransfusion Versus TRAnsfusion in Cancer Surgery

ATTRACS
Start date: January 1, 2021
Phase:
Study type: Observational

Acute bleeding is one of the most frequent intraoperative adverse events and is burdened with a significant morbidity and mortality rate. The only available treatment for severe exsanguination is homologous transfusion, but this is itself complicated by side effects. Nevertheless, systems exist allowing the recovery, treatment and intraoperative reinjection of lost blood, thus limiting transfusions.

NCT ID: NCT04456751 Completed - Transfusion Clinical Trials

Is Redo Pediatric Cardiac Surgery a Risk Factor for Transfusion?

Start date: July 2, 2020
Phase:
Study type: Observational

In pediatric cardiac surgery, transfusion requirements are associated with age, development status, pathology, type of surgical intervention and extracorporeal bypass. In adult cardiac surgery, reinterventions (redo)are clearly linked to higher transfusion rates. The investigators want to study if this association is also true in pediatric cardiac surgery.

NCT ID: NCT04398238 Completed - Iron-deficiency Clinical Trials

Transfusion Rates in Total Hip Replacement Before/After the Implementation of a Patient Blood Management Program.

pbm-hip
Start date: August 1, 2021
Phase:
Study type: Observational

Retrospective observational study: impact of a peri-operative patient blood management program (PBM) on transfusion rates of patients undergoing elective hip replacement.

NCT ID: NCT04349813 Completed - Transfusion Clinical Trials

Perioperative Pediatric Blood Transfusion Therapy

Start date: April 15, 2020
Phase:
Study type: Observational

The present retrospective study analyses perioperative haemotherapy in children and adolescents at the University Hospital Frankfurt.

NCT ID: NCT04304287 Completed - Hip Arthroplasty Clinical Trials

The Benefit of Autologous Blood Transfusion in Total Hip Arthroplasty

Start date: January 16, 2011
Phase: N/A
Study type: Interventional

The investigators studied the benefit of preoperative autologous blood donation in participants who undergo total hip arthroplasty. Study is made as a prospective and randomized.

NCT ID: NCT04282382 Completed - Transfusion Clinical Trials

Intraoperative Transfusion Practice in Children

Start date: March 1, 2020
Phase:
Study type: Observational

The purpose of this study is to examine factors, impact and outcome on perioperative blood transfusion for pediatric patients.

NCT ID: NCT04245995 Completed - Clinical trials for Blood Loss, Surgical

Blood Loss Evaluation Using a Novel Device

Start date: February 5, 2020
Phase:
Study type: Observational

The study´s aim is to evaluate the clinical applicability of the Feature Extraction Technology (FET) during a simulated blood loss scenario.

NCT ID: NCT04141631 Completed - Cardiac Surgery Clinical Trials

Transfusion Savings in Heart Surgery: Impact of Individual Strategy by Erythropoietin and Metabolic Adjustment (ScvO2)

BLOOCOST
Start date: January 13, 2020
Phase: N/A
Study type: Interventional

Preoperative anemia, bleeding and transfusions have been recognized as a "Deadly triad" in cardiac surgery associated with an increased morbidity,mortality, and costs related. Thus strategies to reduce unnecessary RBC transfusions and to optimize preoperative anemia must be developed .The study evaluate an individual blood conservation strategy based on patient blood management bundles in cardiac surgery patients: optimisation perioperative hemoglobin level by erythropoietin and ferric carboxymaltose (Ferinject) associated with the use of ScV02 to guide perioperative erythrocyte transfusion.

NCT ID: NCT03720184 Completed - Anemia Clinical Trials

Haemo-autologous Antegrade Repriming (HAR) as Minimum Impact Perfusion Strategy for Cardiopulmonary Bypass

HARjbm1
Start date: August 15, 2018
Phase: N/A
Study type: Interventional

Haemo-autologous Antegrade Repriming (HAR) is a procedure based in the combination of evidence proven measures designed to reduce the haemodilution caused by establishing the cardiopulmonary bypass (CPB) during cardiac surgery. This clinical trial aims to determinate, in one hand, the benefits related to HAR in terms of transfusion, ICU stay, ventilation time, early mortality and complications. In the other hand analyzes the gaseous microemboli (GME) load, comparing the oxygenators venting technology´s efficiency in treatment and control group, and its relation with patient´s neurocognitive status.