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Heart Valve Diseases clinical trials

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NCT ID: NCT01511991 Completed - Clinical trials for Valvular Heart Disease

Sevoflurane's Effect on Mitral Valve Annular Velocity in Cardiac Surgery

Start date: May 2009
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to determine sevoflurane's dose-dependent effect on left ventricular (LV) function in cardiac surgery. The change of tissue Doppler imaging (TDI) of lateral mitral valve annular velocity at three different sevoflurane concentrations would be analyzed by using intraoperative transesophageal echocardiography (TEE)in cardiac surgery patients.

NCT ID: NCT01495949 Completed - Clinical trials for Coronary Artery Disease

The Cortisol Levels During Cardiac Surgery. The Comparison Between Etomidate and Thiopentone

Start date: December 2011
Phase: Phase 4
Study type: Interventional

During induction for cardiac surgery, patient hemodynamic stability is achieved by using anesthetic drugs which least affects hemodynamics such as benzodiazepines, etomidate. Etomidate although has been used for a long time but its safety regarding cortisol synthesis suppression is still doubtful. This study measures the changes in cortisol levels during cardiac surgery with the use of cardiopulmonary bypass by comparison between two inductive agents (etomidate and thiopentone). Recording data also include hemodynamic changes during induction, inotropic use for coming of cardiopulmonary bypass, blood glucose levels, amount of insulin usage, length of ICU and hospital saty.

NCT ID: NCT01477151 Completed - Clinical trials for Coronary Artery Disease

Randomized Isoflurane and Sevoflurane Comparison in Cardiac Surgery

RISCCS
Start date: November 2011
Phase: Phase 4
Study type: Interventional

Anesthesia practice in the 21st century is increasingly outcomes-oriented and evidence-based, but there remain significant gaps in our knowledge, even for commonly-encountered clinical situations. Currently, the two most commonly used drugs used for maintenance of anesthesia in cardiac surgical patients are isoflurane and sevoflurane. There is a belief among many cardiac anesthesiologists that sevoflurane is a better cardiac anesthetic than isoflurane, but there is very little data to support this notion. In fact, very little is known about their comparative effects on important patient outcomes because there has not been a large head-to-head prospective randomized clinical trial. This project will supply the data necessary to critically compare the two anesthetics.

NCT ID: NCT01476995 Completed - Hypertension Clinical Trials

Prognostic Indicators as Provided by the EPIC ClearView

GBMC
Start date: September 2010
Phase: N/A
Study type: Observational

The objective of this study is to determine whether the finger tip images captured by the EPIC ClearView device, when analyzed via the ClearView software, produce a Response Scale that characterizes trends consistent with known diagnoses identified by medical doctors. Specifically, the investigators hypothesize that the organ system involving any of a series of known active diagnoses will be identified in the EPIC ClearView Response Scale report with the intention of providing potential triage capabilities.

NCT ID: NCT01428947 Completed - Clinical trials for Coronary Heart Disease

Does Coronary Angiography Cause Cognitive Dysfunction?

Start date: September 2011
Phase: N/A
Study type: Observational

The purpose of the study is to study if coronary angiography cause cognitive dysfunction.

NCT ID: NCT01427621 Completed - Clinical trials for Heart Valve Diseases

Effect of Combined Remote Ischemic Preconditioning and Postconditioning on Acute Pulmonary Injury in Patients Undergoing Valvular Heart Surgery

Start date: March 2010
Phase: Phase 4
Study type: Interventional

Pulmonary dysfunction after cardiac surgery with CPB remains to be a problem complicating the postoperative course of the patients. The investigators hypothesized that RIPCcom, combined intervention of remote ischemic preconditioning and remote ischemic postconditioning, would confer beneficial influence on inflammatory response and resultant postoperative pulmonary dysfunction after CPB in patients undergoing complex valvular heart surgery who are at increased risk of postoperative pulmonary dysfunction.The aim of this study was to evaluate the lung-protective effect of combined remote ischemic pre- and post-conditioning in patients undergoing complex valvular heart surgery.

NCT ID: NCT01426776 Completed - Heart Valve Disease Clinical Trials

Effect of Heart Valve Replacement on Cheyne-Stokes Respiration

CSR
Start date: September 2010
Phase: N/A
Study type: Interventional

Sleep disordered breathing, especially central sleep apnea, is common in patients with chronic heart failure. Heart valve replacement could have some effect on central sleep apnea. The aim of the study is to investigate effect of heart valve replacement on Cheyne-Stokes respiration in patients with rheumatic heart disease.

NCT ID: NCT01416792 Completed - Clinical trials for Coronary Artery Disease

Centrifugation vs. Multiple-pass Hemofiltration of the Residual Cardiopulmonary Bypass Volume

Start date: March 2011
Phase: N/A
Study type: Interventional

Traditional cardiac surgery requires patient connection to the Cardiopulmonary Bypass (CPB) apparatus which takes over the function of the heart and lungs while the surgeon performs the necessary surgery. The residual blood left in the CPB equipment (1.5-2.0 L) is centrifuged and washed leaving only red blood cells (RBCs) suspended in a saline solution. The RBCs are reinfused into the patient as needed by the anesthesiologist. The main problem with this technique is that many of the important components of the blood such as plasma proteins and clotting factors are discarded through cell washing. This study will explore a novel method (multiple-pass hemofiltration) of processing the residual pump blood which will allow the patient to receive their own whole blood with minimum waste of important components. The newer method of processing the residual pump volume has also been termed off-line modified ultrafiltration (off-line MUF) and is similar to the process that the kidneys use to filter the blood. It is hypothesized that multiple-pass hemofiltration of the residual CPB volume will reduce the occurrence of inflammatory responses, preserve plasma proteins, and decrease allogenic blood exposure and improve clinical outcomes as compared to centrifugation.

NCT ID: NCT01384643 Completed - Heart Valve Disease Clinical Trials

Effect of Propofol on Renal Injury in Patients Undergoing Valvular Heart Surgery

Start date: May 2011
Phase: Phase 4
Study type: Interventional

Ischemia/reperfusion (I/R)-induced acute kidney injury is a serious complication affecting patient outcome following cardiovascular surgeries. Propofol, an intravenously administered anesthetic with antioxidant properties, protects organs from I/R injury. This study aimed to investigate the ability of propofol to protect kidneys against I/R injury in the patients undergoing valvular heart surgery.

NCT ID: NCT01353287 Completed - Clinical trials for Aortic Valve Disorder

Transcatheter Aortic Valve Intervention-Live Transmission

VERITAS
Start date: May 2011
Phase: N/A
Study type: Observational

The primary objective of this clinical trial is to evaluate safety of patients who underwent Transcatheter Aortic Valve Intervention (TAVI) during a live case or video-taped transmission as compared to those without procedure transmission.