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Blood Loss Anemia clinical trials

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NCT ID: NCT05814094 Not yet recruiting - Clinical trials for Extracorporeal Membrane Oxygenation Complication

Red Blood Cell Transfusion in ECMO - A Feasibility Trial

ROSETTA
Start date: May 2023
Phase: N/A
Study type: Interventional

Extracorporeal Membrane Oxygenation (ECMO) is an invasive and resource intense treatment used to support critically ill patients who have suffered severe cardiac arrest, cardiac failure or respiratory failure (including severe cases of COVID-19). ECMO acts as a mechanical circulatory support temporarily replacing the function of the heart or lungs by oxygenating blood and removing carbon dioxide, allowing time for these organs to recover. Many critically ill patients, including those on ECMO, have an increased risk of bleeding and reduced production/increased destruction of red blood cells (RBCs). This can lead to anaemia (haemoglobin levels <120 g/l), a condition where the body lacks enough healthy RBCs to carry enough oxygen to the body's tissues. Therefore, patients on ECMO frequently require RBC transfusion, with clinicians having to decide if administering an RBC transfusion (with its associated risks) is higher than tolerating complications of anaemia. ROSETTA is a feasibility study that aims to determine the safety and feasibility of randomizing patients on ECMO to a restrictive RBC transfusion strategy (maintain Hb concentration above 70g/L) or to a more liberal transfusion strategy (maintain Hb concentration above 90g/L). Feasibility is defined as the ability to achieve a mean separation of at least 10g/L between the average lowest daily haemoglobin values in the two study groups.

NCT ID: NCT04744181 Completed - Anemia Clinical Trials

Patient Blood Management In CARdiac sUrgical patientS

ICARUS
Start date: January 18, 2021
Phase:
Study type: Observational

Nowadays up to 40% of patients undergoing cardiac surgery receives at least 1 unit of red blood cell transfusion during surgery or during the first week after surgery. Moreover up to 40% of these patients shows an absolute or relative iron deficiency, with or without anaemia. The objective of this study is to assess whether to implement an adequate correction of iron according to current "patients blood management" recommendations might reduce RBC transfusion requirements in patients undergoing heart surgery. Data obtained in patients included in the study will be compared to those of a case-control population selected from patients consecutively treated at the same department in the previous 2 years.

NCT ID: NCT03680456 Recruiting - Blood Loss Anemia Clinical Trials

Postoperative Replacement of Intraoperative Iron Losses

POREIIL
Start date: March 6, 2020
Phase: Phase 4
Study type: Interventional

By performing a randomized, blinded placebo controlled exploratory trial we speculate that replacement of perioperative, bleeding-induced iron losses with ferric carboxymaltose immediately after the surgical procedure can replenish iron with increased hemoglobin levels and reduce the amount of pRBCs transfused in the postoperative period (30 days post surgery).

NCT ID: NCT03578419 Active, not recruiting - Blood Loss Anemia Clinical Trials

Small-Volume Tubes to Reduce Anemia and Transfusion

STRATUS
Start date: January 1, 2019
Phase: N/A
Study type: Interventional

STRATUS will evaluate the use of small-volume ("soft-draw") blood collection tubes for laboratory testing in reducing anemia and transfusion in intensive care unit patients without significant adverse consequences. This is a simple, cost-neutral intervention that could improve the quality of patient care and reduce the harms of frequent laboratory testing.

NCT ID: NCT03468738 Completed - Surgery Clinical Trials

Investigation of the Transfusion Practices in Surgical Patients in Turkey

CeKATU
Start date: April 2, 2018
Phase:
Study type: Observational

The aim of this study is to describe the transfusion practices in patients undergoing major surgery in Turkey. The transfusion rates of red blood cells (RBC), fresh frozen plasma (FFP) and platelets; the transfusion predictors and transfusion related patient outcomes are investigated.

NCT ID: NCT03361124 Withdrawn - Clinical trials for Uterine Atony With Hemorrhage

Oxytocin Dosing at Planned Cesarean Section and Anemia

Start date: March 1, 2019
Phase: Phase 4
Study type: Interventional

Patient's with planned cesarean sections will be randomized to receive either standard 20 mU in 1L as a bolus following delivery of the placenta or 20 mu in 1L following delivery of the placenta plus an additional 20 mU in 1L over 8 hours.

NCT ID: NCT03284944 Completed - Blood Loss Anemia Clinical Trials

Small-Volume Tubes to Reduce Anemia and Transfusion (STRATUS)

Start date: November 1, 2017
Phase:
Study type: Observational

STRATUS will evaluate the use of small-volume ("soft-draw") blood collection tubes for laboratory testing in reducing anemia and transfusion in intensive care unit patients without significant adverse consequences. This is a simple, cost-neutral intervention that could improve the quality of patient care and reduce the harms of frequent laboratory testing.

NCT ID: NCT03037515 Completed - Clinical trials for Blood Loss, Surgical

Oral and Intravenous Tranexamic Acid in Lumbar Spine Surgery

Start date: February 15, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this project is to compare the effectiveness of two different but well accepted routes of administration of tranexamic acid in order to reduce blood loss and need for transfusion in patients undergoing lumbar spine surgery. Specifically, this study seeks to identify if intravenous tranexamic acid is superior to oral tranexamic acid in reducing blood loss and need for transfusion.