About this trial
One significant challenge to non-invasive ventilation (NIV) use in children is finding masks to fit a wide range of growing shapes and sizes. While the technology has improved with development of masks specifically for children, the range of options remains limited. Given the smaller size relative to adults, craniofacial abnormalities and craniofacial differences are more likely to compromise mask fit for children. A poor mask fit is uncomfortable, alters delivery of airway pressure, and, in some children, leads to failure of NIV and the need for surgical insertion of an airway in the neck to deliver positive airway pressure through a tracheostomy. This makes expanding the technology to deliver NIV vital and custom NIV masks an exciting solution.In this study, this study will enroll children who are established on long-term NIV with at least some use within 3 months of starting this therapy but who have non-optimal adherence. After consenting to participate and completing demographic and health questionnaire, participants will undergo a facial scan using stereophotogrammetry. This scan will be imported into a computer-aided design software to create a NIV mask customized to the individual face. The steps of mask testing will include: i) Bench testing to compare the leak and comfort parameters of the current commercial mask used by the participant to the custom mask: ii) Efficacy of treatment as measured by polysomonography iii) NIV compliance from machine downloads; iv) Questionnaires to assess the subjective comfort, fit, and adverse events Finally, participants and their parents/guardian will be asked which mask they prefer and why.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Children between 8-12 years of age
Followed clinically by the Non-invasive ventilation clinic at the Stollery Children's Hospital
Established on non-invasive ventilation as part of their treatment plan.
Disqualifiers
Children with developmental or physical disabilities that would prevent their successful completion of the study protocol (e.g., non-verbal, unable to follow 3-step commands, unalbe to lie still for 20 min).
Children whose parent/guardian are unable to provide consent because of an inability to read the study documents in english.
Trial design
Crossover
Treatments tested in this trial
Custom mask
DeviceCustom mask based on 3D facial photograph for administration of non-invasive ventilation
Current commercial mask
DeviceCurrent commercial mask used for administration of non-invasive ventilation
Treatment groups
Trial outcomes
Primary outcomes
Change in apnea hypopnea index
Polysomnography parameter - apnea hypopnea index
Change in obstructive apnea hypopnea index
Polysomnography parameter - obstructive apnea hypopnea index
Change in oxygen desaturation index
Polysomnography parameter - oxygen desaturation index
Change in percent time with oxygen saturation less than 90%
Polysomnography parameter - percent time with oxygen saturation less than 90%
Secondary outcomes
Change in mask air leak (bench testing)
Unintentional mask leak
Change in mask comfort - participant (visual likert scale, 1-9)
Subjective rating of mask comfort from participant
Change in mask comfort - parent (visual likert scale1-9)
Subjective rating of mask comfort from parent
Mask preference - participant (question)
Participant selection of mask preference with reasons
Sponsors and contacts
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University of Alberta
Lead sponsor
Stollery Children's Hospital
Collaborator