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Clinical Trials/NCT01426178
NCT01426178
Completed
Phase 1

Neurally Adjusted Ventilatory Assist (NAVA) in NonInvasive Ventilation (NIV)

University Hospital, Clermont-Ferrand1 site in 1 country17 target enrollmentJuly 2011

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Respiratory Insufficiency
Sponsor
University Hospital, Clermont-Ferrand
Enrollment
17
Locations
1
Primary Endpoint
Asynchrony rate defined as a percentage of the total respiratory rate
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Main hypothesis is that Neurally Adjusted Ventilatory Assist (NAVA) allows asynchrony reduction in non invasive ventilation (NIV) in comparison with reference Pressure Support (PSV) mode.

The purpose of the protocol is to compare asynchrony rate between periods of pressure support and periods of NAVA.

Detailed Description

After written information and consent, patients are randomised in two groups: NAVA first or PSV first. They receive a NAVA catheter, which has exactly the same appearance as a standard naso-gastric catheter. A standardised set of 1 hour of non-invasive ventilation is started. Depending on the randomisation group, patients start with a 30 minutes set of NIV with NAVA settings or with a 30 minutes set of NIV with PSV settings. A 30-minute watch-out period is then delivered with no mechanical ventilation. Then a second 30-minute set of NIV in the other settings (NAVA or PSV depending on the randomisation) is delivered. During each set of NIV, flow, volume, pressure and EADi are recorded during 10 minutes, after a 10-minute period of equilibration. Recordings will be processed by two blind investigators in order to count the number of asynchronies. In case of disagreement between investigators, a third one will be interviewed.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
January 2012
Last Updated
11 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University Hospital, Clermont-Ferrand
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • - Patient older then 18 years
  • Patient requiring first non invasive ventilation set because of acute respiratory failure

Exclusion Criteria

  • Patients protected by the law
  • Pregnant women

Outcomes

Primary Outcomes

Asynchrony rate defined as a percentage of the total respiratory rate

Time Frame: at 90 minutes

Secondary Outcomes

  • - Number of patients presenting a high asynchrony rate (>10%)(at 90 minutes)
  • Patient comfort(at 90 minutes)
  • Oxygenation evaluated as the PaO2 / FiO2 ratio at the end of considered NAVA set(at 90 minutes)

Study Sites (1)

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