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Clinical Application of Electrical Impedance Tomography for Individual Adjustment of Ventilator Settings

Pilot Clinical Study on Patient-Specific Adjustment of Ventilator Settings Using Electrical Impedance Tomography in Patients With Acute Respiratory Distress Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02703012
Acronym
CLEAR
Enrollment
20
Registered
2016-03-09
Start date
2016-01-31
Completion date
2019-04-04
Last updated
2019-04-19

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

Conditions

ARDS

Brief summary

First clinical application of an algorithm for individual adjustment of ventilator settings using electrical impedance tomography.

Detailed description

In patients suffering from early Acute Respiratory Distress Syndrome (ARDS), an algorithm for individual adjustment of positive end-expiratory pressure and tidal volume will be applied. After optimization of ventilator settings according to the ARDS Network protocol, lung stress and strain, driving pressure, respiratory system compliance (Crs), regional ventilation delay and PaO2 / FiO2 ratio will be recorded. Subsequently, ventilator settings will be adjusted using an algorithm aiming at recruitment and avoiding tidal recruitment and overdistension using electrical impedance tomography (EIT). After 4 hours of EIT-based optimization ventilator settings, lung stress and strain, driving pressure, respiratory system compliance (Crs), regional ventilation delay and PaO2 / FiO2 ratio will be recorded again. The results will be compared to the ARDS Network approach.

Interventions

OTHERAdjustment of ventilator settings by EIT

Diagnostic maneuvers (change in tidal volume, recruitment maneuvers) will be performed to detect overdistention, tidal recruitment and recruitability. Tidal volume will be reduced if overdistention is detected by EIT. Positive end-expiratory pressure will be increased if tidal recruitment or recruitability are detected.

Sponsors

University Hospital Schleswig-Holstein
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

* Acute Respiratory Distress Syndrome (according to Berlin Definition)

Exclusion criteria

* Hemodynamic Instability (defined as mean arterial pressure \< 65 mmHg OR heart rate \< 40 / min OR heart rate \> 150 / min OR cardiac index \< 2.0 l/min/m\^2 DESPITE adequate fluid resuscitation and adequate therapy with inotropes and / or vasopressors) * Thoracic burns or severe skin injuries * High frequency oscillatory ventilation * Pregnancy * Severe chronic obstructive pulmonary disease (GOLD IV) * Esophageal varices \> grade I * Esophageal resection * Invasive ventilation prior to study inclusion for more than 72 hours after onset of ARDS * Inspiratory oxygen requirement \> 80%

Design outcomes

Primary

MeasureTime frameDescription
Stress4 hoursPercentage of patients with lung stress (defined as trans-pulmonary pressure during an end-inspiratory hold) below 27 mbar after 4 hours of adjustment of ventilator settings with the algorithm.
Strain4 hoursPercentage of patients with lung strain (defined as end-inspiratory lung volume divided by functional residual capacity) below 2.0 after 4 hours of adjustment of ventilator settings with the algorithm.

Secondary

MeasureTime frameDescription
Compliance4 hoursRespiratory system compliance (defined as expiratory tidal volume divided by driving pressure) will be measured after 4 hours of adjustment of ventilator settings with the algorithm
Driving Pressure4 hoursDriving Pressure (defined as difference between airway plateau pressure and positive end-expiratory pressure) will be measured after 4 hours of adjustment of ventilator settings with the algorithm
Standard Deviation of regional ventilation delay4 hoursStandard Deviation of regional ventilation delay, (as described in the publication of Muders et al, Crit Care Med Vol. 40, pp 903-911, 2012) will be measured after 4 hours of adjustment of ventilator settings with the algorithm
PaO2 / FiO2 Ratio4 hoursThe ratio between arterial partial pressure of oxygen (PaO2) and fraction of inspired oxygen (FiO2) will be measured after 4 hours of adjustment of ventilator settings with the algorithm

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026