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Pediatric Cardiac Surgery clinical trials

View clinical trials related to Pediatric Cardiac Surgery.

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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: NCT04452539 Completed - Gender Clinical Trials

Gender Influence on Morbi-mortality in Pediatric Cardiac Surgery.

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

Recent studies show an important influence of gender on inflammatory reactions. Cardiac surgery is associated with a major systemic inflammatory response. The investigators want to evaluate the gender influence on morbi-mortality in pediatric cardiac surgery patients.

NCT ID: NCT04380181 Completed - Clinical trials for Pediatric Cardiac Surgery

Influence of Inotropic Choice on Morbidity and Mortality in Complex Pediatric Heart Surgery

CHUBpedCSino
Start date: May 11, 2020
Phase:
Study type: Observational

Our study is based on the observation that management of the cardiopulmonary by-pass withdrawal in pediatric heart surgery is quite variable between medical teams. Indeed, in our center (HUDERF), the most common inotropic plan is dobutamine only or combination of milrinone and adrenalin but their uses seem to be very anesthesiologist dependent. Despite the lack of sufficient evidence, the choice is probably multi-factorial, based mainly on the inotrope pharmacology, the patient physiopathology and the anesthesiologist preference. The aim of this study is to determine if one of these inotropic strategy (dobutamine VS milrinone + adrenaline) is better compared to the other in terms of morbi-mortality. In order to do that, the investigators will realize a retrospective study based on files from January 2008 to December 2018 concerning 250 selected patients.

NCT ID: NCT04254744 Completed - SIRS Clinical Trials

SIRS in Cyanotic and Acyanotic Children in Cardiac Surgery

SIRS
Start date: February 4, 2020
Phase:
Study type: Observational [Patient Registry]

Systemic inflammatory response syndrome (SIRS) is frequently observed in children after open-heart surgery and has been associated with both cardiopulmonary bypass and surgical trauma. Children with congenital cyanotic heart disease (CCHD) have complex changes in all blood values and clotting profiles due to chronic hypoxemia. Increased erythrocyte count decreases plasma and coagulation factors, platelet count and function. Therefore, blood and blood products transfusion may increase during intraoperative and postoperative periods. In addition, durations of cardiopulmonary bypass may prolong due to the complex defects of children with CCHD. The aim of this study is to investigate postoperative SIRS rates and risk factors in cyanotic and acyanotic children undergoing open heart surgery for congenital heart disease.

NCT ID: NCT04208906 Completed - Clinical trials for Pediatric Cardiac Surgery

Masimo O3 Regional Oximetry Device in Pediatric Patients Undergoing Cardiac Surgery

Start date: January 16, 2020
Phase: N/A
Study type: Interventional

We evaluate the relationship between the regional tissue oxygenation value (ScO2 - cerebral, StO2 - lower limb) and mixed venous saturation (SvO2) and arterial oxygen saturation (SaO2) measured before and after correction surgery in pediatric patients undergoing cardiac surgery. In addition, we compared the sCO2 and sTO2 with reference value which is calculated using SvO2 and SaO2.

NCT ID: NCT02656472 Completed - Clinical trials for Pediatric Cardiac Surgery

A Pilot Study Comparing Anti-Inflammatory Effects Of TXA Versus EACA In Pediatric Congenital Heart Surgery

TXAEACA
Start date: February 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare anti-inflammatory effects of two anti-fibrinolyntic drugs (Tranexamic acid versus Epsilon-aminocaproic acid) in pediatric patients undergoing pediatric cardiac surgery.

NCT ID: NCT01600287 Completed - Clinical trials for Intraoperative Awareness

Closed Loop Propofol Administration in Pediatric Cardiac Surgery

Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate and compare the feasibility, efficacy and safety of IAADS (Improved Anaesthetic Agent Delivery System) for propofol anaesthesia against manual control using bispectral index in paediatric patients undergoing open heart surgery under cardio-pulmonary bypass.