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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: NCT02972684 Completed - Blood Transfusion Clinical Trials

Cost-Utility Analysis of Management of Peri Operative Haemorrhage Following Cardiac Surgery With Cardiopulmonary Bypass

IMOTEC
Start date: January 3, 2017
Phase: N/A
Study type: Interventional

Peri operative haemorrhage following cardio Pulmonary Bypass may occur in 5 to 10% of cardiac surgical interventions. Treatment of such complication often necessitates various combinations therapeutic intervention including allogenic blood products administration, drug use and/or surgical intervention. All are expensive treatment and decision making is guided by patient clinical status and biological tests of the haemostatic function. A key point is the time frame of the clinical process. Therapeutic choices have to be done as fast as possible to minimize bleeding consequences on patient haemodynamic and physiological status. Conventional coagulation test results availability time usually exceed 45' after blood drawing. In such situation, the results may not reflect precisely the coagulation system current state. This downside is often counterbalanced by clinicians empirical choices preceding lab test results knowledge that may conduct to inappropriate treatment, blood product overuse and undue expense. Viscoelastic point of care test may compensate for the limitations of conventional coagulation tests. In perioperative haemorrhage, faster and more precise information about haemostatic function may help for more accurate therapeutic choices. The IMOTEC study aims to compare haemorrhage management following cardiac surgery using conventional blood coagulation tests or thrombo-elastogaphic point of care test. Primary endpoint is a cost utility analysis of the technology and secondary endpoints include blood component transfusion, postoperative bleeding , thoracic re-intervention, postoperative infection (any cause), organ failure, in hospital length of stay and death.

NCT ID: NCT02866825 Completed - Clinical trials for Systemic Inflammatory Response Syndrome

Studying Complement Inhibition in Complex Cardiac Surgery

CARDIAC
Start date: May 2016
Phase: Phase 2
Study type: Interventional

The trial enrolls patients undergoing a complex cardiac surgery. The primary goal of the trial is to evaluate the pharmacodynamic dose response relationship of the monoclonal antibody IFX-1 in these patients. In addition, this trial further aims to characterize the safety and the pharmacokinetics of IFX-1 as well as to collect first data on its efficacy on clinical surrogate endpoints.

NCT ID: NCT02831907 Completed - Acute Kidney Injury Clinical Trials

Portal Flow Pulsatility as a Risk Factor for Acute Kidney Injury After Cardiac Surgery

PP-AKI
Start date: August 2016
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the possible association between portal vein flow pulsatility and acute kidney injury after cardiac surgery. Participants will undergo assessment of portal vein flow and intra-renal blood flow using bedside Doppler ultrasound before surgery and daily for three days after cardiac surgery.

NCT ID: NCT02714153 Completed - Clinical trials for C.Surgical Procedure; Cardiac

Bridge Occlusion Balloon in Lead Extraction Procedure

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

To evaluate the use of an occlusion balloon (Bridgeâ„¢ Occlusion Balloon, Spectranetics) within the Superior Vena Cava in lead extraction patients.

NCT ID: NCT02658006 Completed - Acute Kidney Injury Clinical Trials

Evaluation of Monitoring TECHNOlogies in the PERI-OPerative Care of Cardiac Surgical Patients

TechnoPeriOp
Start date: November 2015
Phase: N/A
Study type: Observational

The purpose of this prospective observational cohort study is to evaluate multimodal monitoring technologies in the perioperative care of cardiac surgical patients. Right ventricular pressure tracings, near infrared spectroscopy (NIRS) and transthoracic ultrasonography will be studied for their ability to detect and predict complications such as right ventricular failure, renal failure and respiratory failure.

NCT ID: NCT02571920 Completed - Clinical trials for C.Surgical Procedure; Cardiac

Hemodynamic Monitoring, Positive Inotropic and Vasoactive Drugs During Cardiac Surgery (EMOA)

EMOA
Start date: November 2015
Phase: N/A
Study type: Observational

Describe the proportion of patients who underwent cardiac surgery in France and benefiting from a monitoring cardiac output, describe the use of positive inotropic and vasoactive agents for cardiac surgery patients operated (type of catecholamines, their duration), describe the fluid replacement and transfusions of first 24 hours, describe the incidence of postoperative complications in patients undergoing cardiac surgery.

NCT ID: NCT02560519 Completed - Clinical trials for C.Surgical Procedure; Cardiac

Albumin in Cardiac Surgery

ALBICS
Start date: March 21, 2017
Phase: Phase 4
Study type: Interventional

Colloid solutions are widely used for volume replacement therapy because of their high oncotic pressure, which could reduce interstitial fluid shifting. Human albumin is the only colloid solution of biologic origin with a molecular weight of 60 kDa. As the most abundant plasma protein, it has physiological importance in the well-being of the endothelial glycocalyx. Older studies in septic patients, however, did not show any benefit of albumin over saline solution. Crystalloid solutions, such as Ringer's acetate, do not impair neither renal function nor coagulation, but their volume expanding effect is questionable. For several reasons (use of heart-lung machine, systemic inflammation, coagulation disturbances), patients undergoing cardiac surgery need especially large amounts of fluids. However, there are no large trials comparing albumin solutions to crystalloid solutions cardiac surgery. This double-blinded trial will randomize according to a power analysis 1250 cardiac surgery patients (=625+625) at Meilahti hospital to use either 4% Albumin or Ringer's acetate solutions for both priming of the heart-lung machine and perioperative volume replacement therapy. The primary efficacy and safety endpoint of this study is the incidence of major adverse events (MAE), defined as a composite endpoint of all-cause mortality, acute myocardial infarction, acute heart failure or low output syndrome, resternotomy, stroke, certain arrhythmias, major bleeding, infections compromising post-procedural rehabilitation, acute kidney injury within 90 days postoperatively. The secondary outcomes are total number of MAEs, major adverse cardiac events (MACE), perioperative fluid balance, blood product transfusions, blood loss, acute kidney injury, days alive without mechanical ventilation/outside ICU/at home in 90 days as well as 90-day mortality. Blood samples for biochemical analyses will be collected at four perioperative time points. This trial will provide data about efficacy and safety of 4% albumin in cardiac surgery patients. The biochemical mechanisms of albumin will be assessed.

NCT ID: NCT02513862 Completed - Clinical trials for C.Surgical Procedure; Cardiac

Prospective Trial of Autologous Platelet Rich Plasma in Aortic Surgery

Start date: May 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether autologous platelet rich plasma (APRP)is effective in reducing allogeneic blood transfusions during aortic surgery using deep hypothermic circulatory arrest.

NCT ID: NCT02267538 Completed - Delirium Clinical Trials

Dexmedetomidine and Delirium in Patients After Cardiac Surgery

Start date: November 2014
Phase: Phase 4
Study type: Interventional

Postoperative delirium (POD) is a frequently occurring complication after cardiac surgery. Its occurrence is associated with worse outcomes of patients, including increased morbidity, prolonged hospital stay, increased medical cost, and higher mortality. It is also associated with long-term cognitive decline and decreased quality of life. However, until recently, pharmacological interventions that can effectively prevent its occurrence are still limited. The purpose of this study is to investigate whether perioperative dexmedetomidine use can decrease the incidence of postoperative delirium in patients undergoing cardiac surgery.

NCT ID: NCT02014012 Completed - Clinical trials for C.Surgical Procedure; Cardiac

PWV for Cardiovascular Complication After Cardiac Surgery

Start date: April 2013
Phase: N/A
Study type: Observational

Arterial stiffness has been suggested as an independent risk factor for the development of coronary artery disease and stroke. Pulse wave velocity (PWV) is an noninvasive established index to quantify arterial stiffness. Therefore, we try to investigate the correlation between PWV values and cardiovascular complications like stroke, acute renal failure, or perioperative myocardial infarction after cardiac surgery.