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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06004206
Other study ID # NiVnPSV
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2020
Est. completion date June 15, 2023

Study information

Verified date January 2024
Source ASL Novara
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to evaluate if neural pressure support ventilation is able to improve patient-ventilator synchrony, in ICU patients undergoing non-invasive ventilation (NIV). The main question it aims to answer is: • Is neural pressure support ventilation better than the pressure support ventilation with respect to patient-ventilator synchrony during helmet NIV? Researchers will compare neural pressure support ventilation versus pressure support ventilation (Gold standard assisted mode in Europe) to see if the new mode improve patient-ventilator synchrony.


Description:

Non-Invasive Ventilation (NIV) has found many different uses in clinical settings, shortening intubation times and preventing orotracheal intubation. NIV success is highly affected by patient comfort and patient-ventilator synchrony. The helmet is one of the most comfortable interfaces, even if synchrony is low due to dead space. The use of Neurally Adjusted Ventilatory Assist (NAVA), in which the Electrical Activity of the Diaphragm (EAdi) drives the ventilator, has shown improvement in comfort and synchrony but still some limitation with helmet, due to the long pressurization time. Pressure-Support Ventilation (PSV) is still the most used and diffused assisted mode in Europe due to its simplicity and effectiveness in helmet-NIV. The aim of this study is to test a new ventilation software called Neural Pressure Support Ventilation (nPSV), which merges the rapid pressurization of PSV along with the EAdi trigger, onto a population of 24 critical care patients ventilated with a helmet NIV.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date June 15, 2023
Est. primary completion date June 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients (>18aa) - Non Invasive Ventilation with helmet - NG tubing for clinical use in position - Invasive arterial monitoring for clinical use in position Exclusion Criteria: - Unable to express consent - Expected NIV < 24hrs - Gastric-esophageal surgery in the preceding 12 months - Upper-GI bleeding in the last 30 days - History of esophageal varices - Recent trauma or facial surgery - Haemodynamic instability even a after liquid infusion (need of at least dopamine >5 ?/kg/min or norepinephrine >0.1 ?/kg min to obtain systolic pressure >90 mmHg) - Core temperature >30 C° - Coagulation disorders (INR > 1.5 and/or aPTT >44 sec)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
nPSV and PSV
Ventilation with neurally adjusted modes or pressure support modes

Locations

Country Name City State
Italy SS. Trinità Hospital Borgomanero Novara

Sponsors (1)

Lead Sponsor Collaborator
ASL Novara

Country where clinical trial is conducted

Italy, 

References & Publications (6)

Colombo D, Cammarota G, Bergamaschi V, De Lucia M, Corte FD, Navalesi P. Physiologic response to varying levels of pressure support and neurally adjusted ventilatory assist in patients with acute respiratory failure. Intensive Care Med. 2008 Nov;34(11):20 — View Citation

Evans TW. International Consensus Conferences in Intensive Care Medicine: non-invasive positive pressure ventilation in acute respiratory failure. Organised jointly by the American Thoracic Society, the European Respiratory Society, the European Society o — View Citation

Muttini S, Villani PG, Trimarco R, Bellani G, Grasselli G, Patroniti N. Relation between peak and integral of the diaphragm electromyographic activity at different levels of support during weaning from mechanical ventilation: a physiologic study. J Crit C — View Citation

Navalesi P, Costa R, Ceriana P, Carlucci A, Prinianakis G, Antonelli M, Conti G, Nava S. Non-invasive ventilation in chronic obstructive pulmonary disease patients: helmet versus facial mask. Intensive Care Med. 2007 Jan;33(1):74-81. doi: 10.1007/s00134-0 — View Citation

Squadrone E, Frigerio P, Fogliati C, Gregoretti C, Conti G, Antonelli M, Costa R, Baiardi P, Navalesi P. Noninvasive vs invasive ventilation in COPD patients with severe acute respiratory failure deemed to require ventilatory assistance. Intensive Care Me — View Citation

Vignaux L, Vargas F, Roeseler J, Tassaux D, Thille AW, Kossowsky MP, Brochard L, Jolliet P. Patient-ventilator asynchrony during non-invasive ventilation for acute respiratory failure: a multicenter study. Intensive Care Med. 2009 May;35(5):840-6. doi: 10 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Blood gas analysis pH level pH (-log10H+) At the end of each 30-minutes trial
Other Blood gas analysis Oxygen level Concentration of Arterial Oxygen Partial Pressure [PaO2] (mmHg) At the end of each 30-minutes trial
Other Blood gas analysis Carbon Dioxide level Concentration of Arterial Carbon Dioxide Partial Pressure [PaCO2] (mmHg) At the end of each 30-minutes trial
Other Blood gas analysis Bicarbonate level Concentration of Sodium Bicarbonate [HCO3-] (mEq/L) At the end of each 30-minutes trial
Other Blood gas analysis Lactate level Concentration of Lactate [Lac] (mmol/L) At the end of each 30-minutes trial
Primary Improvement of synchrony in nPSV v.s PSV Synchrony time [Timesych]: time frame during which both the ventilator and the neural patient inspiratory time are in the inspiratory phase (s) last 2 minutes over 30 minutes registration
Secondary Tidal Volume Tidal Volume (ml) last 2 minutes over 30 minutes registration
Secondary Minute Volume Minute Volume Ventilation (L) last 2 minutes over 30 minutes registration
Secondary Respiratory rate Respiratory Rate (Breath per minute) last 2 minutes over 30 minutes registration
Secondary Inspiratory time Inspiratory Time [Ti] (s) last 2 minutes over 30 minutes registration
Secondary Neural Inspiratory Time Neural Inspiratory Time [Tineu] (s) last 2 minutes over 30 minutes registration
Secondary Inspiratory Neural-Ventilator Coupling Inspiratory Neural-Ventilator Coupling [NCVi] (Percentage): i.e. the time frame during which both the ventilator and the neural signal are into inspiratory phase last 2 minutes over 30 minutes registration
Secondary Peak of Electrical Activity of the diaphragm Peak of Electrical Activity of the diaphragm [EAdi peak] (mcV) last 2 minutes over 30 minutes registration
Secondary Asynchrony index Asynchrony Index (AI): ratio between the number of ineffective efforts, auto-triggers and double triggers and the neural respiratory rate plus auto-triggers (percentage) last 2 minutes over 30 minutes registration
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