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Hemodynamics clinical trials

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NCT ID: NCT03033810 Recruiting - Hemodynamics Clinical Trials

FFR Versus iFR in Assessment of Hemodynamic Lesion Significance

FiGARO
Start date: January 2017
Phase: N/A
Study type: Observational

The study will compare two invasive methods (FFR -fractional flow reserve and iFR—instantaneous wave free ratio) for assessment of hemodynamic impact of coronary stenosis on myocardial perfusion. There is a very good correlation between these methods for the assessment of hemodynamic significance in a broad spectrum of lesions. However, this correlation decreases significantly near the cut off points for each method. The investigators will try to find possible explanations for these differences by detailed morphology assessment of coronary stenosis using optical coherence tomography (OCT), analysis of gene polymorphisms that play a role in vasodilatation, and by shear stress analysis. The head-to-head comparison between FFR and iFR is not simple, because there is no "gold standard" for assessment of hemodynamic significance. Studies comparing these methods have used hyperemic stenosis resistance (HSR). For this kind of measurement it is necessary to measure the speed of blood flow. This is usually done by a Doppler analysis of flow. Unfortunately, the Doppler signal can yield many artificial or erroneous indicators, and obtaining a good quality signal is frequently time-consuming. These are the reasons that HSR has not been used in routine practice. The investigators have developed a new console and software that can provide real time analysis of the Doppler signal. It allows us to easily measure HSR, and to differentiate between the FFR and iFR measures through intrabeat analysis of microvascular resistance (lowest microvascular resistance is an essential condition for proper pressure measurement). Using this tool, it is possible to automatically identify the point of lowest microvascular resistance during each cardiac beat. The pressure gradient can then be measured at that point. This approach can eliminate almost all uncertainties in assessment of the pressure gradient produced by coronary stenosis. This tool can potentially improve the existing methods used to precisely reveal a significant stenosis. This should increase the number of hemodynamic guided procedures.

NCT ID: NCT02979327 Completed - Hemodynamics Clinical Trials

Cardiovascular Effects of Adderall in Healthy Adults.

Start date: June 1, 2018
Phase: Early Phase 1
Study type: Interventional

This study is designed to investigate the cardiovascular response (blood pressure, heart rate, electrocardiographic response and blood vessel reactivity response) to taking Adderall in healthy adults.

NCT ID: NCT02902068 Completed - Hemodynamics Clinical Trials

Hemodynamic Monitoring in Women Throughout Cesarean Sections

Start date: May 2016
Phase:
Study type: Observational

In this study we would like to monitor cardiac output by the use of NICAS bioimpedance in women undergoing cesarean section delivery. This study is a purely observational study, it will not have any clinical intervention nor will it interfere with standard cesarean delivery protocols in any way. This study's primary objective is to evaluate how spinal and general anesthesia influences cardiac output during cesarean section deliveries. Secondary endpoints is whether the hemodynamic changes as measured in cardiac output correlate with women's pain, measured by a visual analogue scale(VAS) from o-10. (0=representing no pain at all, 10= worse pain imaginable)

NCT ID: NCT02807610 Completed - Hemodynamics Clinical Trials

Etomidate vs Propofol-Induction Characteristics

Induction
Start date: March 2011
Phase: Phase 4
Study type: Interventional

The ideal induction agent for day care surgery should have properties of rapid, smooth induction, better haemodynamic profile, faster recovery and devoid of side effects in the form of pain on injection, involuntary movements, respiratory depression and post-operative nausea/vomiting. Propofol is the drug being used for day care surgeries because of its rapid, smooth induction and faster recovery. But its use is associated with pain on injection (even with added lidocaine), hypotension and respiratory depression. So the need for an agent with better hemodynamic control and lesser side effects was felt. The introduction of etomidate lipuro revolutionised the anaesthesia practice. It possesses many of the properties of an ideal induction agent. This newer formulation of etomidate in lipid emulsion i.e. etomidate lipuro is known to have rapid, smooth induction, haemodynamic stability and lesser side effects than older etomidate with propylene glycol (hypnomidate). Hence, investigators devised a prospective randomized controlled open trial and compared this newer lipid formulation of etomidate with propofol in terms of - induction time, haemodynamic parameters and side effect profile.

NCT ID: NCT02571465 Completed - Hemodynamics Clinical Trials

Assessment of Fluid Responsiveness in Patients After Cardiac Surgery

POP
Start date: April 2015
Phase: N/A
Study type: Observational

To overcome the limited accuracy of functional hemodynamic parameters such as stroke volume and pulse pressure variation (SVV and PPV) during spontaneous breathing, a Passive Leg Raising (PLR) manoeuvre has been suggested as a reliable predictor of fluid responsiveness. Aim of this study was to evaluate fluid responsiveness using SVV, PPV and PLR during the transition from controlled to spontaneous breathing in cardiac surgery patients

NCT ID: NCT02495662 Terminated - Renal Dialysis Clinical Trials

The LIPMAT Study: Liposomal Prednisolone to Improve Hemodialysis Fistula Maturation

LIPMAT
Start date: November 2015
Phase: Phase 2
Study type: Interventional

This study will investigate if liposomal prednisolone is effective in promoting arteriovenous fistula (AVF) maturation when administered to human subjects after surgical creation of a radio-cephalic AVF.

NCT ID: NCT02441621 Not yet recruiting - Hemodynamics Clinical Trials

Prediction of Volume Responsiveness in Presence of Left Ventricular Diastolic Dysfunction

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

The ability of the global end-diastolic volume index (GEDVI), stroke volume variation (SVV) and pulse pressure variation (PPV) for prediction of fluid responsiveness in presence of left ventricular diastolic dysfunction is still unknown. The aim of the present study was to challenge the predictive power of GEDVI, SVV and PPV in cardiac surgery patients undergoing aortic valve replacement.

NCT ID: NCT02267291 Completed - Hemodynamics Clinical Trials

Impact of Non-invasive Positive Pressure Ventilation on Cardiac Function and Echocardiographic Parameters

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

Cardiologists and intensive care specialists are confronted daily with mechanically ventilated patients exhibiting cardiac failure. It is of paramount importance to understand the effect of mechanical ventilation on cardiac function and to interpret echocardiographic findings correctly in order to provide the patient with the best possible treatment to support cardiac and circulatory function. Currently physicians interpret echocardiographic findings based on studies that were performed in spontaneously breathing patients. With this study, the investigators intend to contribute to the understanding of cardiac physiology in patients needing ventilatory support, especially they aim to provide the physiological basis for the interpretation of echocardiographic findings in order to improve medical support (e.g. fluid resuscitation, vasoactive drugs, ventilation strategy) of ventilated patients with impaired cardiovascular function.

NCT ID: NCT02202239 Not yet recruiting - Anesthesia Clinical Trials

Effect of Induction and Maintenance of Anesthesia With Etomidate on Hemodynamics and Oxidative Stress in Diabetic Patients

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

To explore the effect of induction and maintenance of anesthesia with etomidate on hemodynamics and oxidative stress in diabetic patients.

NCT ID: NCT02147678 Not yet recruiting - Sedation Clinical Trials

A Comparison Between Propofol and Etomidate in Hysteroscopy on Effect of Postoperative Sedation and Cognitive Function in Elderly Patients

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

To compare the effect of propofol and etomidate in hysteroscopy on postoperative sedation and cognitive function in elderly patients