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C.Surgical Procedure; Cardiac clinical trials

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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: 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: 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: 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: NCT02119806 Withdrawn - Delirium Clinical Trials

Decreasing the Incidence of Delirium After Cardiac Surgery

Start date: August 2017
Phase: Phase 4
Study type: Interventional

In critically ill surgical patients, delirium (confusion and disorientation) is extremely common and is associated with longer hospital length of stay, mortality, cost, and long term cognitive impairment. The goal of the study is to establish whether benzodiazepines (a sedative, anti-anxiety drug) should be used as part of standard of care or be eliminated by comparing the chances of delirium in cardiac surgery patients between two groups: a group that receives benzodiazepines during surgery versus a group that does not receive benzodiazepines during surgery. Benzodiazepines have historically been used in cardiac anesthesia to decrease the risk of anesthesia awareness. The current standard of care is to keep the patient on inhaled anesthesia throughout the surgery which eliminates the need for intraoperative use of benzodiazepines. Benzodiazepines are still used based on practitioner preference. Findings of this study will allow all anesthesiologists to make more informed decisions about what level of care our patients need.

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.