Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02778620
Other study ID # M12-1270
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2013
Est. completion date January 2015

Study information

Verified date December 2019
Source Catharina Ziekenhuis Eindhoven
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine fluid responsiveness in critically ill patients by measuring mean systemic filling pressure on the intensive care unit.


Description:

The assessment of the cardiovascular state in critically ill patients is subject to difficulties in terms of the fact that several hemodynamic parameters, for example mean arterial blood pressure (MAP) and cardiac output (CO) supply insufficient information about the circulating volume and cardiac performance. There is a clinical need to adequate determination of intravascular volume status and therefore reliable predictors of fluid responsiveness are highly relevant. However, in determining the fluid status of a patient, the lack of appreciation of the venous side of the circulation persists today, which is greatly due to the inability to appropriately assess the venous side of the circulation. The importance of the venous part of the circulation is moreover reflected by the fact that an increase in venous resistance does reduce CO many times more than a similar increase in arterial resistance. Mean systemic filling pressure (Pms), which is defined as the pressure equal to the pressure which would be measured if the heart should suddenly stop pumping and all (arterial and venous) the pressures in the entire circulatory system should be brought to equilibrium instantaneously, is a good, complete and reliable reflection of the total intravascular fluid compartment. Passive leg raising (PLR) represents a "self-volume challenge" that predicts preload responsiveness and the transient hemodynamic changes on venous return can be directly monitored in ventilated patients, provided that there is an intact circulation, in order to test the amount of volume responsiveness.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients must be older than 18 years, and must be equipped with a pulse-contour cardiac output system with a central venous catheter.

- Patients will be subsequently connected to the hemodynamic monitoring device Navigatorâ„¢.

- In those patients with clinical signs of inadequate tissue perfusion, passive leg raising and standardized fluid challenge will be performed.

Exclusion Criteria:

- Patients with assist devices (e.g. intra aortic balloon pump, Impella®, ECMO), patients with arrhythmias (either atrial of ventricular) will be excluded from the study.

- Also, patients with inguinal impairment or contraindications for a passive leg raising will be excluded (such as deep venous thrombosis or elastic compression stocking), head trauma, an increase intra-abdominal pressure suspected by clinical context and examination as well as patients with absolute contraindications for fluid challenge.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Netherlands Catharina Hospital Eindhoven North Brabant

Sponsors (2)

Lead Sponsor Collaborator
Catharina Ziekenhuis Eindhoven Erasmus Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Other Heart Rate Heart Rate in bpm 1 hour
Other MAP Mean Arterial Blood Pressure 1 hour
Other CI Cardiac Index 1 hour
Other CVP Central Venous Pressure 1 hour
Other SVR Systemic Vascular Resistance 1 hour
Other PPV Pulse Pressure Variation 1 hour
Other PVPI Pulmonary Vascular Permeability Index 1 hour
Other pO2 Plethysmographic Oxygen Saturation 1 hour
Other DO2I Delivery of Oxygen Index 1 hour
Other Ventilation Mechanical Ventilation Settings 1 hour
Other etCO2 End-tidal CO2 1 hour
Other Temp perif Peripheral Temperature 1 hour
Primary Mean systemic filling pressure (Pms) An increase in mean systemic filling pressure after (self)volume-challenge indicating volume responsiveness of the patient 1 hour
Secondary Heart performance (eH) Quotient of driving pressure of venous return in mmHg 1 hour
See also
  Status Clinical Trial Phase
Completed NCT05070819 - Atrial Natriuretic Peptide in Assessing Fluid Status N/A
Completed NCT06039397 - The Effect of Semi Fowler 30' Right Lateral on Cardiac Output in Acute Heart Failure N/A
Recruiting NCT05492968 - The Effect of Epinephrine, Norepinephrine and Phenylephrine on Intraoperative Hemodynamic Performance Phase 4
Completed NCT03444545 - Continous Cardiac Output - Non-Invasive Evaluation (CONNIE)
Recruiting NCT04064177 - Non-invasive Continuous Cardiac Output Monitoring in Preterm Infants Study
Withdrawn NCT03058653 - Use of a Mini-fluid Bolus to Identify Fluid Responsiveness N/A
Completed NCT04955184 - Comparing Cardiac Output Measurements Using a Wearable, Wireless, Non-invasive PPG-Based Device to a Swan Ganz Catheter
Recruiting NCT04755764 - Effect of Labetalol, Atenolol, and Nifedipine on Maternal Hemodynamics Measured by ICG in Early Pregnancy
Completed NCT01880684 - Validation of Capnography as a Predictor of Cardiac Output Change as Measured by FloTrac Phase 2
Completed NCT02312505 - Comparison of a New Semi-invasive Monitoring System With Transpulmonary Thermodilution in Cardiac Surgery Patients N/A
Completed NCT04111237 - Rescuer Fatigue Using Two Thumb Versus Two Finger Method During Simulated Neonatal Cardiopulomnary Resuscitation N/A
Enrolling by invitation NCT05441007 - The Effect of Hypercapnia on Physiological Parameters During Short-term Breathing N/A
Recruiting NCT04885699 - Validation of Capnodynamic Assessment of Mixed Venous Oxygen Saturation
Completed NCT00354211 - Using Minimally Invasive Cardiac Output Data vs. Standard Care for Patients Emergently Admitted to the Intensive Care Unit Who Are Hemodynamically Unstable Phase 4
Completed NCT04358822 - Hemodynamic Effects of Delayed Umbilical Cord Clamping in Full-term Newborns N/A
Completed NCT03046784 - Non-invasive Haemodynamic Monitoring in Pregnancy
Not yet recruiting NCT05646342 - PLR in a Good Helath After 24 Week of Preganancy
Completed NCT00583687 - Pulse Contour Analysis and Tissue Oxymetry in Changing Vascular Tone N/A
Completed NCT05428384 - Validation of CardioMEMS HF System Cardiac Output Algorithm IDE
Completed NCT03021525 - Individualized Perioperative Hemodynamic Goal-directed Therapy in Major Abdominal Surgery (iPEGASUS-trial) N/A