N-WATCH: Nottingham Wheeze Assessment in Tidal Children

  • Research type

    Research Study

  • Full title

    N-WATCH: Nottingham Wheeze Assessment in Tidal Children - Harnessing Capnograms for Airway Health – Feasibility Observational Study

  • IRAS ID

    342058

  • Contact name

    Andrew Prayle

  • Contact email

    andrew.prayle@nottingham.ac.uk

  • Sponsor organisation

    The Univeristy of Nottingham

  • Duration of Study in the UK

    0 years, 8 months, 27 days

  • Research summary

    Children with long-term lung diseases like asthma need better techniques for diagnosis and monitoring of their disease. With better monitoring, it is anticipated that children and their carers will be able to manage their disease better, and be able to spot a deterioration in their condition sooner, leading to earlier intervention, for example to prevent an asthma attack.

    However, current devices which could be used at home are either too costly, require machines that are impractically large, or require specific breathing maneuvers which are unpopular with patients, or which are difficult for younger children to perform. There is a need for better devices.

    The N-Tidal C is a CE Marked medical device which measures exhaled carbon dioxide levels accurately. Early work in its use in adult diseases such as Chronic Obstructive Pulmonary Disease indicates that the device can detect altered lung function associated with disease.

    This device has several attractive properties for children – it is small, easy to use, and does not require specific breathing maneuvers – just normal breathing.

    Based on data from a small feasibility study, we believe that this device will be useful in children. Young children can use it with minimal instruction. Parents and children have reported that it is easy to use.

    We do not yet have sufficient feasibility information required to plan a larger study, such as deciding how many children we will need to recruit, or knowing how well the measurements made with the device agree with standard lung function tests.

    In this application, we are conducting a feasibility study to determine the number of children needed for a larger trial and to explore how well the N-Tidal C device measurements compare with standard lung function tests. Data from this study will be used to plan future larger studies of the device in children with respiratory diseases.

  • REC name

    West Midlands - Black Country Research Ethics Committee

  • REC reference

    24/WM/0159

  • Date of REC Opinion

    26 Jul 2024

  • REC opinion

    Further Information Favourable Opinion