Functional respiratory imaging in bronchiectasis

  • Research type

    Research Study

  • Full title

    Functional respiratory imaging during pulmonary exacerbations in adults with bronchiectasis

  • IRAS ID

    251721

  • Contact name

    Timothy Baird

  • Contact email

    timothy.baird@nhs.net

  • Sponsor organisation

    Royal Papworth Hospital NHS Foundation Trust

  • Clinicaltrials.gov Identifier

    NCT03818646

  • Duration of Study in the UK

    0 years, 3 months, 0 days

  • Research summary

    This study is a prospective single centre exploratory pilot study in adults with bronchiectasis.

    The aim of the study is to determine whether Functional Respiratory Imaging (FRI), a novel image-based tool, can be used to assess treatment response in individuals with bronchiectasis suffering a chest exacerbation. The study will endeavor to recruit 10 adult patients who have a known diagnosis of bronchiectasis, attend the Cambridge Centre for Lung Infection at The Royal Papworth Hospital, Cambridge, and are suffering a chest exacerbation.

    The study will involve 4 separate visits over a 28-day period followed by a follow-up phone call at day 35. The study will not alter the usual treatment for a chest exacerbation in any way, however will incorporate 3 trial-specific CT scans (FRI) and 2 questionnaires at days 0, 14 and 28. A summary of the study schedule is outlined below.

    • Day 0: Usual treatment commencement – clinical review; sputum collection; blood test; breathing test; 2 questionnaires; CT scan (FRI)

    • Day 7: Day 7 of treatment – clinical review, blood test

    • Day 14: Day 14 of treatment (end of treatment) – clinical review; blood test; breathing test; 2 questionnaires; CT scan (FRI)

    • Day 28: Post treatment follow up – clinical review; blood test; breathing test; 2 questionnaires; CT scan (FRI)

    • Day 35: Follow up phone call – post completion of the study testing

    We hypothesise that changes in FRI will be seen pre and post treatment of a chest exacerbation and will correlate well with traditional trial end points including lung function, blood markers of infection, and patient reported outcomes (questionnaires / quality of life measures). This will confirm FRI as a useful and novel tool for assessing treatment response in future clinical trials in bronchiectasis patients.

  • REC name

    East of England - Cambridge East Research Ethics Committee

  • REC reference

    19/EE/0006

  • Date of REC Opinion

    5 Mar 2019

  • REC opinion

    Further Information Favourable Opinion