The PARS Study: Paediatric Advanced Respiratory Service Study - An Observational Diagnostic Feasibility Study
Summary
Diagnostic investigations in paediatric respiratory and sleep medicine are often challenging due to patient size (due to prematurity), tolerability, and compliance with "gold standard equipment". Children with sensory/behavioural issues, at increased risk of sleep disordered breathing (SDB), often find tolerating standard diagnostic equipment difficult. There is a need to develop non-invasive, wireless, devices designed for the paediatric population. Devices must address health in-equalities as
Eligibility
Inclusion Criteria: Group 1 - CR-poly group * Patient undergoing overnight CR-poly * Age birth to \>=16 years * Are willing and able to give informed assent/consent or have available next of Kin to provide informed consent on the participant\'s behalf * Able (in the Investigators op
Locations
Interested in participating? View the full study details on ClinicalTrials.gov:
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