Hemodynamics Clinical Trial
Official title:
Impact of Non-invasive Positive Pressure Ventilation on Cardiac Function and Echocardiographic Parameters
NCT number | NCT02267291 |
Other study ID # | 104/14 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2015 |
Est. completion date | February 2018 |
Verified date | October 2018 |
Source | University Hospital Inselspital, Berne |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Cardiologists and intensive care specialists are confronted daily with mechanically ventilated patients exhibiting cardiac failure. It is of paramount importance to understand the effect of mechanical ventilation on cardiac function and to interpret echocardiographic findings correctly in order to provide the patient with the best possible treatment to support cardiac and circulatory function. Currently physicians interpret echocardiographic findings based on studies that were performed in spontaneously breathing patients. With this study, the investigators intend to contribute to the understanding of cardiac physiology in patients needing ventilatory support, especially they aim to provide the physiological basis for the interpretation of echocardiographic findings in order to improve medical support (e.g. fluid resuscitation, vasoactive drugs, ventilation strategy) of ventilated patients with impaired cardiovascular function.
Status | Completed |
Enrollment | 30 |
Est. completion date | February 2018 |
Est. primary completion date | February 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Age = 18 to = 75 years - Indication for a coronary angiogram - Written informed consent obtained - Adequate echocardiographic imaging quality - • Patient tolerates a face mask for non-invasive ventilation Exclusion Criteria - Acute coronary syndrome - Previous myocardial infarction or open heart surgery - Severe obstructive or restrictive pulmonary disease - Pulmonary hypertension - Diastolic dysfunction = grade II - Valvular heart disease > grade I - Left ventricular ejection fraction < 50% - Complete left or right bundle branch block - Cardiac pacemaker or defibrillator - Atrial fibrillation or frequent premature beats - INR > 3.0 or haemoglobin < 90g/l - Glomerular filtration rate < 45ml/min/1.73m2 - Esophageal disorders |
Country | Name | City | State |
---|---|---|---|
Switzerland | Department of Cardiology, Bern University Hospital | Bern | BE |
Lead Sponsor | Collaborator |
---|---|
University Hospital Inselspital, Berne |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Left ventricular diastolic function | Assessed by pressure volume loops | Under spontaneous breathing and at two levels of positive pressure ventilation, 5 minutes after changing positive end-expiratory pressure | |
Secondary | Left ventricular contractility | Assessed by pressure volume loops | Under spontaneous breathing and at two levels of positive pressure ventilation, 5 minutes after changing positive end-expiratory pressure | |
Secondary | Cardiac function | Assessed by echocardiography | Under spontaneous breathing and at two levels of positive pressure ventilation, 5 minutes after changing positive end-expiratory pressure | |
Secondary | Invasively measured alterations in hemodynamics | Alterations of invasively measured hemodynamic parameters including cardiac output and pulmonary artery, right ventricular and right atrial pressures | Under spontaneous breathing and at two levels of positive pressure ventilation, 5 minutes after changing positive end-expiratory pressure |
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