Cardiac Output, High Clinical Trial
Official title:
Mean Systemic Filling Pressure and Heart Performance as Predictors of Successful Fluid Responsiveness in Patients With Aortic Valve Replacement
| 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 |
| Verified date | December 2019 |
| Source | Catharina Ziekenhuis Eindhoven |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
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.
| 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 Navigator™. - 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. |
| Country | Name | City | State |
|---|---|---|---|
| Netherlands | Catharina Hospital | Eindhoven | North Brabant |
| Lead Sponsor | Collaborator |
|---|---|
| Catharina Ziekenhuis Eindhoven | Erasmus Medical Center |
Netherlands,
| 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 |
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