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The BRIDGE Study - Bronchiectasis Research Involving Databases, Genomics and Endotyping

Sponsor: University of Dundee

NCT ID: NCT03791086

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 87 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
1,000
Started
2019-11-01
Last checked
2023-03

Plain English Summary

What is this study?

  • • Testing a new treatment for bronchiectasis adult
  • • Clinical study - 1,000 participants
  • • Bronchiectasis is a complex heterogeneous disorder

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with bronchiectasis adult

Where?

  • • Dundee - University of Dundee

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Bronchiectasis is a complex heterogeneous disorder. Treatment is challenging and many recent randomized controlled trials have been negative. It is believed that bronchiectasis as a broad diagnosis incorporates multiple different patient subgroups (also known as phenotypes) and molecular entities (referred to as endotypes). This study aims to phenotype and endotype bronchiectasis during stable disease and exacerbations, to develop strategies for personalised medicine. Primary Objective To determine molecular endotypes of bronchiectasis which can guide response to treatment. Secondary Objectives 1. To determine molecular endotypes of stable bronchiectasis 2. To determine the causes and inflammatory profiles of bronchiectasis exacerbations 3. To validate candidate biomarkers of stable and exacerbation endotypes to use in stratified medicine 4. To perform in-vivo or in-vitro proof of concept studies using phenotypic data to identify patient populations likely to benefit in future randomized controlled trials This is an observational cohort study that will aim to identify patient subgroups and link these with meaningful clinical outcomes.

More detail

Background: Bronchiectasis is a common disabling and heterogeneous disease that has been neglected in terms of basic and clinical research. Recent controlled trials have failed to achieve their primary end-points, likely because the optimal patient population to benefit from antibiotic, mucoactive and anti-inflammatory drugs has not been identified. This study aims to explore the clinical, microbiological, inflammatory and functional heterogeneity of the disease with the aim of identifying patient endotypes for stratified medicine. Study aims and objectives 1. To determine the molecular endotypes of bronchiectasis during stable disease 2. To determine the causes and inflammatory profiles of bronchiectasis exacerbations 3. To validate candidate biomarkers of stable and exacerbation endotypes to use in stratified medicine 4. To perform in-vivo or in-vitro proof of concept studies using phenotypic data to identify patient populations likely to benefit in future randomized controlled trials Study Design: Observational Cohort study Study methods: Patients with bronchiectasis will be recruited into an observational study, the objectives of which will be to: Aim 1 will define and validate endotypes of stable bronchiectasis by studying up to 1000 patients with bronchiectasis. Clinical data, sputum microbiome, sputum proteomics, and systemic and sputum inflammatory marker measurement will be incorporated for analysis. A sub-study (n=200) will be performed using air liquid interface culture of primary airway epithelial cells. Patients will have brushings of the inferior nasal turbinate with assessment of % ciliation, ciliary beat frequency and pattern by high speed video microscopy before and after culture. Aim 2 will replicate the phenotyping approach to stable patients with 160 patients during exacerbation. This will identify changes from baseline in microbiota, proteomic and other markers associated with onset of exacerbation and allow classification of clusters of exacerbation. Aim 3, we will externally validate candidate phenotype/endotypes in registered ethically approved external biobanks and aim to demonstrate that validated markers to be linked to potential treatment responses for use in stratified medicine trials. In total we will recruit 1000 patients for study. These patients will attend the Clinical Research Centre at one of the participating study centres at least once and undergo sampling along with collecting of clinical data. Patients will be asked to consent for their samples to be linked to data held on the EMBARC registry. Nature of outputs and outcomes/results expected: This study will aim to establish detailed endotypes in bronchiectasis which can guide response to treatment.

Bronchiectasis Adult

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓A previous CT scan showing bronchiectasis along with compatible clinical syndrome of cough, sputum production and/or...
  • ✓A primary diagnosis of bronchiectasis made by a respiratory physician

Who cannot take part

  • ✗Inability to give agreement to take part
  • ✗\<18years of age
  • ✗Patients with active tuberculosis
  • ✗Treatment with antibiotics or corticosteroids for a lung exacerbation in the previous 4 weeks
  • ✗Bronchiectasis due to cystic fibrosis
See the full criteria
Inclusion Criteria: * A previous CT scan showing bronchiectasis along with compatible clinical syndrome of cough, sputum production and/or recurrent respiratory tract infections. * A primary diagnosis of bronchiectasis made by a respiratory physician * At the screening visit the individual will have been clinically stable for 4 weeks indicated by the lack of any treatment with antibiotics or corticosteroids for a pulmonary exacerbation in the previous 4 weeks. Exclusion Criteria: * Inability to give informed consent * \<18years of age * Patients with active tuberculosis * Treatment with antibiotics or corticosteroids for a pulmonary exacerbation in the previous 4 weeks * Bronchiectasis due to cystic fibrosis

Where Is This Study? (1 UK site)

University of Dundee

Dundee DD1 9SY, United Kingdom

Recruiting
Site contact (verified)
James D Chalmers, MD,PhD01382660111james.chalmers@nhs.scot

How to Get in Touch

James D Chalmers, MD, PhD

Sponsor contact

CONTACT

01382660111 james.chalmers@nhs.scot

Amelia Shoemark, PhD

Sponsor contact

CONTACT

01382660111 a.shoemark@dundee.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2023-03