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C.Surgical Procedure; Cardiac clinical trials

View clinical trials related to C.Surgical Procedure; Cardiac.

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NCT ID: NCT03913481 Recruiting - Clinical trials for C.Surgical Procedure; Cardiac

Acute Normovolemic Hemodilution in High Risk Cardiac Surgery Patients.

ANH
Start date: April 15, 2019
Phase: N/A
Study type: Interventional

Transfusions are one of the most overused treatments in modern medicine, and saving blood is one important issue all around the world. Cardiac surgery makes up a large percentage of the overall blood components consumption in surgery. Acute normovolemic hemo-dilution (ANH) is a well-known strategy which has been used for years without the support of high quality evidence based medicine to improve post-cardiopulmonary bypass coagulation and reduce red blood cells (RBC) transfusion. We designed a multicenter randomized controlled trial to investigate the effect of ANH in reducing the number of cardiac surgery patients receiving RBC transfusions during hospital stay. We will randomize 2000 patients to have sufficient power to demonstrate a 20% relative and 7% absolute risk reduction in the number of patients' RBC transfusion. If the results of the study will confirm our hypothesis, this will have a great impact on blood management in cardiac operating room.

NCT ID: NCT03884725 Recruiting - Clinical trials for Blood Coagulation Disorders

Fibrinogen Concentrate In Children Cardiac Surgery 2

FiCCS2
Start date: March 1, 2019
Phase: Phase 4
Study type: Interventional

The purporse of this study is evaluate whether fibrinogen concentrate reduces postoperative bleeding in pediatric cardiac surgery with cardiopulmonary by-pass.

NCT ID: NCT03882593 Recruiting - Clinical trials for Blood Coagulation Disorders

Blood Cell Adhesion to Arterial Filters During Cardiac Surgery

Start date: August 30, 2018
Phase:
Study type: Observational

Cardiopulmonary bypass (CPB) is a unique clinical scenario that results in widespread activation of the hemostatic system. Conventional CPB interferes with normal hemostasis by diluting hemostatic cells and proteins, through reinfusion of shed blood, and through activation on the bypass circuit surface of multiple systems including platelets, the kallikrein-kinin system, and fibrinolysis . Besides, deleterious effects of cardiopulmonary bypass (CPB) are partly sequelae of blood-foreign surface reactions. The arterial filter is the part of the CPB circuit where blood cells are exposed to high mechanical stress and where cellular aggregates may fasten in large quantitiesiec.

NCT ID: NCT03469440 Recruiting - Clinical trials for C.Surgical Procedure; Cardiac

Goal Directed Therapy Aiming to Optimise Oxygen Central Venous Saturation in Children Undergoing Cardiac Surgery

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is evaluate goal-directed therapy with continuous central venous saturation compared to standard therapy in children undergoing cardiac surgery.

NCT ID: NCT02908009 Recruiting - Clinical trials for C.Surgical Procedure; Cardiac

A Case Control Study to Identify the Role of Epigenetic Regulation of Genes Responsible for Energy Metabolism and Mitochondrial Function in the Obesity Paradox in Cardiac Surgery

Ob-Card
Start date: September 9, 2016
Phase:
Study type: Observational

This is a prospective, single-centre case control comparison of expression of target genes responsible for energy utilisation, mitochondrial function and oxidative stress and levels of histone acetylation/ DNA methylation in obese and non-obese adult cardiac surgery patients. The study aims to test several inter-related hypotheses in a consecutive sequence of patients undergoing coronary artery bypass grafting.

NCT ID: NCT02745951 Recruiting - Clinical trials for C.Surgical Procedure; Cardiac

HELIox CardiOPlegia Trial During Cardiac surgERy

HELICOPTER-1
Start date: April 2016
Phase: N/A
Study type: Interventional

The HELICOPTER-1 Trial is a single centre pilot study to determine the feasibility of administering Heliox in cardioplegia during cardiac surgery and whether it has the potential to reduce the incidence and severity of myocardial ischemia during and after cardiac surgery.

NCT ID: NCT02560285 Recruiting - Clinical trials for C.Surgical Procedure; Cardiac

High-risk Patients in Cardiac Surgery Procedures: HiriSCORE

HiriSCORE
Start date: January 2016
Phase: N/A
Study type: Observational [Patient Registry]

Over time there is a need to improve old and develop new risk models. Overall the assessment of mortality risk in cardiac surgery is performed with the use of preoperative risk models. The use of improved risk models and increased accuracy in the technique of preparing these mathematical systems does not have a positive impact on the level of prediction, which is still inaccurate, especially in the considered group of high risk. New models need to be built not only for a better prediction of mortality risk, if not also to predict morbidity in the group of patients at higher risk of complications after cardiac surgery procedures. The aim of this study is: - To construct the HiriSCORE to identify patients at higher risk of complications after cardiac surgery procedures - Assessing the impact of pre-, intra- and postoperative period to the prognosis of morbidity and mortality in high-risk patients undergoing cardiac surgery procedures.

NCT ID: NCT01879475 Recruiting - Clinical trials for C.Surgical Procedure; Cardiac

Safety and Performance of 032-11 Haemostat in Cardiac and Thoracic Aortic Surgery

Start date: June 2013
Phase: N/A
Study type: Interventional

The effectiveness objective of this study is to evaluate whether 032-11 is non-inferior to Floseal as an adjunct to achieving haemostasis during surgical procedures involving cardiac and aortic thoracic surgery.