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The PARS Study: Paediatric Advanced Respiratory Service Study - An Observational Diagnostic Feasibility Study

Recruitingn/aAges 1 Minute - 16 YearsAllNHS Greater Clyde and Glasgow
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In plain words

What the trial is, and whether it could suit you

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 high-risk children, with low birth weights, genetic syndromes, or complex neuro-disabilities, are often unable to undergo current investigations, particularly in sleep medicine. Prompt and accurate diagnosis of SDB is important to facilitate early intervention and improve outcomes Infants in the neonatal period can have immature breathing control which manifests as excessive central breathing pau

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: Group 1 - CR-poly group * Patient undergoing overnight CR-poly * Age birth to \&amp;gt;=16 years * Are willing and able to give informed assent/consent or have available next of Kin to provide informed consent on the participant\&amp;#39;s behalf * Able (in the Investigators opinion) to comply with all study requirements * Can speak and read English Group 2 - Apnoea group * Inpatient in neonatal unit * Age birth (from 30 weeks gestational age) to term corrected * Parents willing and able to give informed consent * Able (in the Investigators opinion) to comply with all study requirements * Can speak and read English Group 3- VT Group attending epilepsy monitoirng unit * Inpatient receiving video-telemetry epilepsy monitoring unit * Age birth to \<16 years * Parents willing and able to give informed consent * Able (in the Investigators opinion) and willing to comply with all study requirements * Can speak and read English Exclusion Criteria: Group 1 - CR-poly group * Unable to provide consent and no next of kin to provide consent on participants behalf * Treating clinician deems patient inappropriate to be included in study Group 2 - Apnoea group * No next of kin to provide consent on participants behalf * Treating clinician deems patient inappropriate to be included in study Group 3- VT Group attending epilepsy monitoirng unit * Unable to provide consent and no next of kin to provide consent on participants behalf * Treating clinician deems patient inappropriate to be included in study
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What it tests

  • Pneumowave
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Where

2 sites
Royal Hospital for Children, Glasgow
Glasgow, United Kingdom
Royal Hospital for Children, Glasgow
Glasgow, United Kingdom
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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