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Mechanical Insufflator/Exsufflator Technique in Children With Neuromuscular Disease

Mechanical INsufflator/EXsufflator Technique in Paediatric Subjects With Neuromuscular Disease: a Randomised Crossover Comparison of 2 Modes of Application

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05454215
Acronym
MINEX-2
Enrollment
7
Registered
2022-07-12
Start date
2023-02-01
Completion date
2024-12-20
Last updated
2025-01-08

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

Conditions

Neuromuscular Diseases in Children

Keywords

Lung function

Brief summary

In a randomized cross-over design, two different modes of a mechanical insufflator/exsufflator applied to pediatric subjects with neuromuscular disease will be compared with respect to their short term effect on lung function, i.e. lung volume.

Detailed description

At two consecutive regular outpatient clinic visits, each participant will perform a session of the insufflation/exsufflation technique. Participants will be randomised by a computer-generated code to one of the two sequences (CON-MOD or MOD-CON) using sealed envelopes. The randomisation list will be generated by a study nurse of the Department of Paediatrics who is not a member of the study group. The randomisation envelope will be opened by the treating physiotherapist immediately before the first treatment session. Standardised intervention At randomisation, the measurement belt of the EIT system will be fitted around the chest of the participant. Once correct fit is confirmed, the baseline measurement (T0) will be taken. After the baseline assessment, the participants will perform the conventional (CON) or modified (MOD) insufflator/exsufflator therapy session under supervision of a physiotherapist. In teh investigator's institution a therapy session consists of 5 series of 5 insufflation/exsufflation manoeuvres each (Cough assist E70, Philips Respironics, Hamburg, Germany). Positive and negative pressures will be set at the individual level of each subject. Measurements Changes in lung volume and ventilation distribution will be assessed by electrical impedance tomography (EIT). These parameters will be obtained five minutes before (T0) and five, ten, twenty, forty and sixty minutes after the treatment session (T1 - T5). Measurements of 3 minutes will be recorded at each time point. Additionally EIT measurements will be performed continuously during the treatment session. Electrical Impedance Tomography (EIT) is a non-invasive, radiation-free technique for the assessment of spatial and temporal ventilation distribution based on the changes in electrical properties of the tissue during the respiratory cycle. EIT measurements will be performed using a commercially available setup (PulmoVista 500, Draeger, Germany). Image reconstruction will be performed with the GREIT-algorithm using the torso mesh function. \[Adler, 2009\] Relative change in end-expiratory lung impedance (EELI) and the global inhomogeneity (GI) index, a measure of ventilation inhomogeneity, will be calculated using customized software (Matlab® R2021b, The MathWorks Inc., Nattick, MA, USA).

Interventions

DEVICEMechanical insufflation/exsufflation conventional

Conventional settings in a commercially available chest physiotherapy device

DEVICEMechanical insufflation/exsufflation modified

Modified settings in a commercially available chest physiotherapy device

Sponsors

Insel Gruppe AG, University Hospital Bern
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Single center non-blinded randomized crossover trial

Eligibility

Sex/Gender
ALL
Age
5 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

* Confirmed diagnosis of a NMD * Functional status: non-ambulatory * Age \>5 years and \< 16 years * Able to cooperate * Daily home-use of cough assist as reported by the caregivers * Written informed consent by the subject/caregiver

Exclusion criteria

* Acute respiratory infection at two consecutive outpatient clinic visits (marked increase in cough, change in sputum amount or colour, fever or malaise) * Oxygen dependency (defined as need for oxygen to achieve a transcutaneous oxygen saturation of ≥92%) * Skin lesions at the chest (preventing EIT measurements) * Chest deformation preventing EIT measurements

Design outcomes

Primary

MeasureTime frameDescription
Change in end-expiratory lung impedance from baseline3-5 MinutesChange of end-expiratory lung volume estimated by electrical impedance tomography from baseline to immediately after a session of mechanical insufflation/exsufflation.

Secondary

MeasureTime frameDescription
Change in ventilation distribution from baseline3-5 MinutesDifferences in ventilation distribution assessed with electrical impedance tomography from baseline to immediately after a session of mechanical insufflation/exsufflation.
Duration of effect15-20 minutesDuration of the postulated effect on lung volume assessed by electrical impedance tomography.

Countries

Switzerland

Outcome results

None listed

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