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Study on Ventilation Distribution With Electrical Impedance Tomography for Paediatric Respiratory Failure

Study on Ventilation Distribution With Electrical Impedance Tomography for Paediatric Respiratory Failure: Impact of Intervention

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05347563
Acronym
PELUCHE1
Enrollment
250
Registered
2022-04-26
Start date
2022-06-18
Completion date
2027-06-01
Last updated
2026-01-23

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

Conditions

Acute Respiratory Failure

Keywords

Electrical impedance tomography, Children, Pediatric intensive care unit

Brief summary

Electrical impedance tomography (EIT) is a non-invasive, bedside monitoring technique that provides continuous, real-time information about the regional distribution of the ventilation. There are very few data in children admitted to the PICU (pediatric intensive care unit) and the aim of the study is to describe the distribution of the ventilation in children with acute respiratory failure and to study the impact of the interventions in the PICU (change in ventilatory settings, change in position, suction, respiratory kinesiotherapy,…)

Detailed description

Children with acute respiratory failure admitted to the PICU (pediatric intensive care unit)

Interventions

PROCEDUREElectrical impedance tomography

All change in ventilator settings (mode, tidal volume or inspiratory pressure, Peep, recruitment…)

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

Groupe A * children \< 18 years * Admitted to the PICU with acute respiratory failure * Monitoring with EIT * non opposition of parents or legal representative Groupe B * children \< 18 years * With general anesthesia and mechanical ventilation * Monitoring with EIT * non opposition of parents or legal representative

Exclusion criteria

* Monitor not available * contra indication to the use of thoracic belt * Intraoperative period with use of electrocautery * Child not affiliated to a social security system and under protective measures legal

Design outcomes

Primary

MeasureTime frameDescription
Distribution of Ventilationup to 48 hoursDistribution of ventilation as determined by changes in impedence in region of interest

Countries

France

Contacts

CONTACTFlorent Baudin, MD
florent.baudin@chu-lyon.fr04 72 12 97 05
PRINCIPAL_INVESTIGATORFlorent Baudin, MD

Hospices Civils de Lyon

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026