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Hemodynamic Instability clinical trials

View clinical trials related to Hemodynamic Instability.

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NCT ID: NCT01792037 Completed - Clinical trials for Hemodynamic Instability

Single Dose of Etomidate and Adrenal Cortex

Start date: December 2012
Phase: Phase 4
Study type: Interventional

we aim to evaluate the effects of single dose of etomidate or use of steroid prior to etomidate during emergency intubation on hemodynamics and adrenal cortex.

NCT ID: NCT01792011 Completed - Clinical trials for Hemodynamic Instability

Accuracy of the Pleth Variability Index to Predict Fluid Responsiveness in Liver Transplantation

Start date: October 2012
Phase: Phase 4
Study type: Interventional

The aim of this study is to compare the accuracy of PVI (pleth variability index)

NCT ID: NCT01605279 Completed - Clinical trials for Hemodynamic Instability

Dobutamine Versus Placebo for Low Superior Vena Cava Flow in Newborns

Start date: September 2010
Phase: Phase 2
Study type: Interventional

Low systemic flow as measured by Doppler-echocardiography has been associated with poor neurological outcome. Yet, it has not been systematically evaluated whether the treatment of this hemodynamic condition is beneficial or not. This study aims to evaluate if treating low systemic flow in preterm infants with dobutamine has any effect on the cerebral circulation and in newborn prognosis.

NCT ID: NCT01569308 Completed - Clinical trials for Hemodynamic Instability

Pulse Pressure Variation Helps to Predict Fluid Responsiveness in Patients Ventilated With Low Tidal Volumes

Start date: May 2006
Phase: N/A
Study type: Observational

Objective: To determine the value of pulse pressure variation (ΔRESPPP) to predict fluid responsiveness in patients ventilated with low tidal volumes (VT), and to investigate whether a lower ΔRESPPP cut-off point should be used when patients are ventilated with low tidal volumes. Methods: This cross-sectional, observational study included 37 critically ill patients with acute circulatory failure requiring fluid challenge. They were sedated and mechanically ventilated with Tidal Volume (VT) 6-7 ml/kg IBW (ideal body weight), monitored by pulmonary artery catheter and arterial line. Mechanical ventilation and hemodynamic parameters, including ΔRESPPP, were measured before and after fluid challenge with 1,000 ml crystalloids or 500 ml colloids. Fluid responsiveness was defined as an increase of at least 15% in cardiac index. The present study was designed to (1) determine the value of ΔRESPPP to predict fluid responsiveness in patients ventilated with low tidal volumes, and (2) to investigate whether a lower ΔRESPPP cut-off point should be used when patients are ventilated with low tidal volumes. The study hypothesis is not a good predictor of fluid responsiveness in patients ventilated with low tidal volumes.

NCT ID: NCT01559675 Completed - Fever Clinical Trials

Trial Comparing Low Dose and High Dose Steroids in Patients Undergoing Colorectal Surgery

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

The purpose of this study is to evaluate the effect of low dose versus high dose steroids vital signs of patients currently on steroids or recently treated with steroids undergoing major colorectal surgery. The investigators hypothesize that there will be no statistically significant difference in orthostatic hypotension (blood pressure measured on lying, sitting, and standing), blood pressure, temperature or heart rate in the standard and low dose groups.

NCT ID: NCT01498380 Completed - Clinical trials for Hemodynamic Instability

The Bolus Dose of Dexmedetomidine (ED50) That Avoids Hemodynamic Compromise in Children

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

Dexmedetomidine is a sedative drug that has many benefits when given to children under anesthesia, such as improved pain relief and reduced agitation following their surgery. It is usually given as an intravenous infusion over 10 minutes, to avoid the changes in heart rate and blood pressure that are occasionally seen when it is administered more quickly. However, this is often infeasible and usually inconvenient. The investigators aim to determine the dose of dexmedetomidine that can be given rapidly (over 5 seconds) without causing significant changes in heart rate and blood pressure. This will be the only study specific intervention.

NCT ID: NCT01117519 Completed - Clinical trials for Hemodynamic Instability

Impact of Fluid Management Within a Goal-directed Hemodynamic Protocol on Acid-base Balance in Elective Trauma Surgery

HIPSTER
Start date: May 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the administration of a compound of balanced infusion solutions including 50% crystalloid and 50% colloid has a positive impact on acid-base balance in elective hip replacement surgery. The application of the study medication will be carried out through a goal-directed intraoperative therapy by transoesophageal doppler.

NCT ID: NCT00766519 Completed - Surgery Clinical Trials

Effect of Intraoperative Volume Optimization on Outcome After Intrabdominal Surgery

EVOLUTION
Start date: February 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether intraoperative goal-directed fluid management (with goal = cardiac stroke volume maximization) based on respiratory-induced pulse pressure variation monitoring may improve outcome after intrabdominal surgery