Clinical Trials Logo

Fluid Responsiveness clinical trials

View clinical trials related to Fluid Responsiveness.

Filter by:

NCT ID: NCT04223414 Completed - Clinical trials for Fluid Responsiveness

Ability of Changes in Analgesia Nociception Index to Assess the Stroke Volume Effects of a Volume Expansion of 250ml of Crystalloid in the Operating Room

REVANI
Start date: January 29, 2020
Phase:
Study type: Observational

Volume expansion is the cornerstone of perioperative hemodynamic optimization. The main objective of volume expansion is to increase and maximize stroke volume. Hemodynamic changes have an impact on the autonomic nervous system. The analysis of heart rate variability allows an exploration of the autonomic nervous system and could therefore provide information on the effect of volume expansion. The Analgesia Nociception Index (ANI) is an analgesia monitor based on the concept of heart rate variability. By deviating from its original use, the investigators wish to evaluate the ability of ANI to identify a response to volume expansion.

NCT ID: NCT04186416 Recruiting - Hemorrhage Clinical Trials

Effectiveness of the Pressure Recording Analytical Method in Predicting Fluid Responsiveness in Pediatric Critical Care Patients

MOSTCARE-PED
Start date: May 3, 2023
Phase:
Study type: Observational

The Pressure Recording Analytical Method, invasive hemodynamic monitoring, is an uncalibrated pulse contour analysis, installed in the Mostcare® system that allows a continuous estimation of the stroke volume and thus the cardiac output, by the relationship between the area under the curve of the systolic portion of the arterial blood pressure curve and the dynamic impedance of the cardiovascular system. The objectives of the study are to determine if the parameters measured by Mostcare® make it possible to predict the response to volume expansion in pediatric surgical critical care patients, sedated, intubated and ventilated, by comparing the changes in stroke volume, induced by a volume expansion, measured by trans-thoracic echocardiography.

NCT ID: NCT04092036 Not yet recruiting - Shock Clinical Trials

Optic Nerve Sheath Diameter in Prediction of Fluid Responsiveness

Start date: October 15, 2019
Phase:
Study type: Observational [Patient Registry]

The aim of the study to examine Optic Nerve Sheath Diameter measurement for prediction of fluid responsiveness in hemodynamically unstable patients

NCT ID: NCT04060069 Completed - Clinical trials for Fluid Responsiveness

Pneumoperitoneum and Trendelenburg Position on Fluid Responsiveness

Start date: October 1, 2016
Phase:
Study type: Observational

The increased intraabdominal pressure and intrathoracic pressure due to pneumoperitoneum negatively affect the cardiovascular system, relatively dynamic parameters may vary due to intraoperative fluid therapy.

NCT ID: NCT04030221 Not yet recruiting - Clinical trials for Fluid Responsiveness

Pressure Gradient for Venous Return in Predicting Fluid Responsiveness in Patients Undergoing Laparoscopic Surgery

Start date: July 20, 2019
Phase:
Study type: Observational

Surgical patients, especially those with insufficient blood volume and hypotension, often need fluid therapy. However, there is still a lack of simple and reliable indicators for judging transfusion responsiveness in some types of surgery. Previous studies have shown that Pressure Gradient for Venous Return (PVR) can be used to guide infusion. Thus, our aim is to explore the relationship between PVR and liquid reactivity.

NCT ID: NCT04002193 Completed - Clinical trials for Fluid Responsiveness

Pleth Variability Index in Modified Prone Position or Knee-chest Position (Concord Position)

Start date: December 6, 2019
Phase:
Study type: Observational

To investigate whether PVI predicts the fluid responsiveness in modified prone position undergoing posterior approach cervical operation. Furthermore, modified prone position could influence on dynamic variables including stroke volume variation(SVV), pulse pressure variation(PPV) and PVI.

NCT ID: NCT03938220 Completed - Sepsis Clinical Trials

Electrical Cardiometry Compared to Transthoracic Echocardiography in Fluid Responsiveness in Sepsis

Start date: June 1, 2019
Phase:
Study type: Observational

The aim of this study is to evaluate the diagnostic accuracy of electrical cardiometry (EC) for the noninvasive determination of fluid responsiveness in sepsis and agreement of (EC) compared to transthoracic echocardiography (TTE).

NCT ID: NCT03932617 Completed - Shock Clinical Trials

Correlation Between Changes in End-Tidal Carbon Dioxide and Stroke Volume Variation Detected by Electrical Cardiometry as A Predictor of Fluid Volume Responsiveness in Hemodynamically Unstable Patients in the Intensive Care

Start date: June 1, 2019
Phase:
Study type: Observational

This study will be conducted to assess the role of end-tidal carbon dioxide (PETCO2) monitoring to predict the fluid volume responsiveness in correlation with stroke volume variation detected by electrical cardiometry in patients with hemodynamic instability.

NCT ID: NCT03713008 Completed - Anesthesia Clinical Trials

Assessment Of Carotid Flow During General Anesthesia

Start date: October 22, 2018
Phase: N/A
Study type: Interventional

Proper identification of patients who would benefit from fluid infusion (fluid responsiveness) is one of the most crucial challenges in anaesthesia and critical care. Reliability of several invasive measurements used for this purpose for many years have been questioned recently. The study will evaluate consistency between carotid artery flow derivatives and standard haemodynamic measurement (LIDCO rapid) in navigation of intraoperative fluid therapy.

NCT ID: NCT03499860 Completed - Clinical trials for Fluid Responsiveness

Prediction of Fluid Responsiveness From Passive Leg Raising Induced Changes in Perfusion Index and Pleth Variability Index

Start date: April 20, 2018
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate whether changes in Perfusion Index (PI) and Pleth Variability Index (PVI) during passive leg raising test can predict fluid responsiveness in spontaneously breathing patients. Fluid responsive patients are defined as showing an increase in cardiac output >10% during a passive leg raising test, measured semi-invaseively with FloTrac® (Edwards LifeSciences. Irvine, United States).