Neurally Adjusted Ventilatory Assist for Non Invasive Ventilation and Patient-ventilator Interaction
- Conditions
- Non Invasive VentilationPatient Ventilator Interaction
- Interventions
- Device: Neurally Adjusted Ventilatory Assist
- Registration Number
- NCT01074866
- Lead Sponsor
- University Hospital, Geneva
- Brief Summary
The present study aims to compare various parameters reflecting patient-ventilator synchrony during standard pressure support (PS) and Neurally Adjusted Ventilatory assist (NAVA) in a group of patients receiving non invasive ventilation (NIV)for an episode of acute respiratory failure of various origin.
- Detailed Description
The present study aims to compare various parameters reflecting patient-ventilator synchrony during standard pressure support (PS) and Neurally Adjusted Ventilatory assist (NAVA) in a group of patients receiving non invasive ventilation (NIV)for an episode of acute respiratory failure of various origin. The subgroup of COPD patients will be analyzed separately. The effects of various setting of Neurally adjusted ventilatory assist on patient-ventilator interaction will also be explored.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 13
- Patients admitted to the ICU and treated with Non invasive ventilation for acute respiratory failure of any origin
- severe hypoxemia requiring an FIO2>0.6
- hemodynamic instability
- known oesophageal problem
- active upper gastro-intestinal bleeding
- any other contraindication to the insertion of a naso-gastric tube
- impaired consciousness or absence of patient cooperation
- facial or laryngeal lesions contraindicating the use of NIV
- poor short term prognosis
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Neurally Adjusted Ventilatory Assist Neurally Adjusted Ventilatory Assist Non invasive ventilation under Neurally Adjusted ventilatory Assist
- Primary Outcome Measures
Name Time Method Patient-ventilator synchronization parameters
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (4)
CHUV University hospital of Lausanne
🇨🇭Lausanne, Switzerland
St Luc University hospital
🇧🇪Brussels, Belgium
HUG, University Hospital
🇨🇭Geneva, Switzerland
Bernard Lambermont
🇧🇪Liege, Belgium