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Fluid Responsiveness clinical trials

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NCT ID: NCT06087250 Completed - Clinical trials for Fluid Responsiveness

Carotid Artery Corrected Flow Time and Fluid Responsiveness in Geriatric Patients

Start date: August 1, 2023
Phase:
Study type: Observational

Carotid blood flow and corrected carotid flow time (Carotid Flow Time (FTc)) provide information about left ventricular preload and inversely correlate with systemic vascular resistance. The reliability in assessing fluid responsiveness has been demonstrated in studies involving invasive cardiac output measurements. In the elderly patient population where arterial elasticity can be compromised, there is no existing data in literature that determines the reliability and predictive value of FTc after general anesthesia induction.

NCT ID: NCT05419570 Completed - Clinical trials for Fluid Responsiveness

Short Time Low PEEP Challenge and Mini Fluid Challenge

Start date: June 20, 2022
Phase:
Study type: Observational

Optimizing fluid therapy is one of the main concerns for anesthesiologists during the intraoperative period. It becomes even more important in high-risk long lasting surgeries as pancreaticoduodenectomy. Therefore evaluating fluid responsiveness prior to fluid loading is highly recommended. To the best of our knowledge there is no study comparing the abilities short time low PEEP challenge and mini fluid challenge in predicting fluid responsiveness.

NCT ID: NCT05131516 Completed - Clinical trials for Fluid Responsiveness

Peripheral Venous Pressure Variation and Fluid Responsiveness

Start date: January 10, 2022
Phase:
Study type: Observational

The decision to give fluids or not should not be taken lightly. Indeed, excessive or insufficient fluid administration is associated with increased morbidity and mortality. Prediction of fluid responsiveness relies on the use of a hemodynamic variable to determine how likely a patient is going to respond to a fluid bolus with a significant increase in their cardiac output or stroke volume. Depending on the response to fluids, patients are either responders or non-responders. Today, we have many techniques to predict fluid responsiveness. However, almost all require the use of an advanced hemodynamic monitoring device.

NCT ID: NCT04889807 Completed - Clinical trials for Fluid Responsiveness

Study of End Tidal Carbon Dioxide (EtCO2) Variation After an End- Expiratory Occlusion Test as a Predictive Criteria of Fluid Responsiveness in Mechanically Ventilated Patients

CapnoPause
Start date: May 5, 2021
Phase:
Study type: Observational

Hypovolemia is one of major factor of haemodynamic instability. Fluid administration is not totally riskless. Indeed, it can create or inflate pulmonary oedema, alter gaz exchanges and increase post operative respiratory complications. Furthermore, fluid administration is not always followed by a cardiac output increase. Predicting preload responsiveness before administering fluid by reliable and reproductible methods is necessary in critically ill patients. Dynamic indicators are approved at the bedside such as passive raising leg test, pulse pressure variation, respiratory variation of the diameter of the superior vena cava. However, all these tests cannot be used for all patients. For example in the cases of spine or pelvis injury, or traumatic brain injury, patients with difficult condition for transthoracic echography. The investigators hypothesize that EtCO2 (end tidal carbon dioxide) variation after an 15 seconds end-expiratory occlusion test could predict fluid responsiveness in mechanically ventilated patients in the intensive care units. EtCO2 is a parameter which can be easy to collect, reproductible, and totally non invasive. This method could be especially appropriate for patients for whom the classical test of fluid responsiveness cannot be used

NCT ID: NCT04802668 Completed - Clinical trials for Fluid Responsiveness

Factors Influencing of Pulse Pressure Variation (PPV)

FacPPV
Start date: March 20, 2021
Phase:
Study type: Observational

The investigators studied the predictive value of PPV in the patients with different influencing factors;and the method to improve the predictive value,which can improve the application of PPV in ICU.

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: 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: 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.