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Comparison of Proportional Assist Ventilation And Neurally Adjusted Ventilator Assist

Breathing Pattern Variability, Respiratory Discomfort and Work of Breathing in Proportional Assist Ventilation And Neurally Adjusted Ventilator Assist

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02056093
Acronym
PAVANAVA
Enrollment
16
Registered
2014-02-05
Start date
2013-09-30
Completion date
2014-02-28
Last updated
2014-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Failure

Keywords

NAVA - PAV- Breathing Variability - Asynchrony

Brief summary

In spontaneously breathing mechanically ventilated patients, the adequacy between the patient's demand and the level of respiratory support delivered by the ventilator is a major clinical issue. Neurally adjusted ventilator assist (NAVA) and proportional assist ventilation (PAV) have been developed to adapt the level of assistance to the patient's demand. These two modes have been compared to pressure support ventilation (PSV) but have not been compared to each other.

Interventions

DEVICEPSV mode

Application of PSV in all patients

DEVICEPAV mode

Application of PAV mode in all patients

DEVICENAVA

Sponsors

Pierre and Marie Curie University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Intubated patients. * Mechanical ventilation for a respiratory reason. * Expected duration of Mechanical ventilation \> 48 hrs. * Spontaneous breathing. * Sedations stopped for more than 24 hours.

Exclusion criteria

* \- Main contra indications to NAVA: gastro-oesophageal surgery in the previous 12 months, oesophageal obstruction, gastro-esophageal bleeding in the previous 30 days, history of esophageal varices, facial trauma or surgery, neuromuscular diseases, individuals with known or suspected phrenic nerve dysfunction. * Main contra indications to PAV: airway leak, body weight \<25 kg, neuromuscular diseases. * Hemodynamic instability defined as the current administration of vasopressors or inotropic drugs. * Severe hypoxemia defined as PaO2/FiO2 ratio \<200. * Decision to withhold life-sustaining treatment. * Pregnant women. * Minors \< 18 years.

Design outcomes

Primary

MeasureTime frameDescription
Breathing pattern variabilityFebruary 2014The coefficient of variation (standard deviation divided by the mean) of the tidal volume (expressed in %)

Secondary

MeasureTime frameDescription
Patient-ventilator asynchronyFebruary, 2014Prevalence of ineffective efforts and double triggering (expressed as a number of events per minute)

Other

MeasureTime frameDescription
Electrical diaphragm activity Gas exchangeFebruary 2014measured by the NAVA probe

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026