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The London COPD Exacerbation Cohort

Sponsor: Imperial College London

NCT ID: NCT02755974

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 215 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
40 Years to 100 Years
Who
All
Number of participants
300
Started
2009-01
Last checked
2022-06

Plain English Summary

What is this study?

  • • Testing a new treatment for pulmonary disease, chronic obstructive
  • • Clinical study - 300 participants
  • • The London COPD exacerbation (EXCEL) cohort builds on an established cohort started in 1995 and designed to study COPD exacerbations and their impact on health-status and disease progression

Who can take part?

  • • Ages 40 Years to 100 Years
  • • Diagnosed with pulmonary disease, chronic obstructive

Where?

  • • London - National Heart and Lung Institute, Imperial College

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

About This Trial

The London COPD exacerbation (EXCEL) cohort builds on an established cohort started in 1995 and designed to study COPD exacerbations and their impact on health-status and disease progression.

More detail

Our intentions are to phenotype Chronic Obstructive Pulmonary Disease (COPD) patients on the basis of factors that a related to (a) exacerbation frequency which will include (b) lung function to assess disease severity, (c) baseline therapy, (d) airway and systemic inflammatory markers, (e) health status, (f) gene expression, (g) airway bacterial and viral load and (h) co-morbidity including cardiovascular disease, diabetes and psychological disease, (i) psychological factors,(j) mortality, (k) nasal susceptibility to rhinovirus infection, (l) heart rate variability (m) exhaled hydrogen sulphide.

Pulmonary Disease, Chronic Obstructive

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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Still need:

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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: 40 Years - 100 Years
  • Who can join: All genders

What the study is looking for

  • ✓Forced Expiratory Volume in 1 sec (FEV1)/Forced Vital Capacity (FVC) ratio of \<0.70
  • ✓Able and willing to give informed and written consent

Who cannot take part

  • ✗Patients with a history of asthma, bronchiectasis, carcinoma of the bronchus, or other significant respiratory...
  • ✗Patients on Immunosuppressive medications or with active cancer
  • ✗Long term steroid therapy
  • ✗Age \<40 years at recruitment
See the full criteria
Inclusion Criteria: * Forced Expiratory Volume in 1 sec (FEV1)/Forced Vital Capacity (FVC) ratio of \<0.70 * Able and willing to give informed and written consent Exclusion Criteria: * Patients with a history of asthma, bronchiectasis, carcinoma of the bronchus, or other significant respiratory disease were excluded. * Patients on Immunosuppressive medications or with active cancer * Long term steroid therapy * Age \<40 years at recruitment

Where Is This Study? (1 UK site)

National Heart and Lung Institute, Imperial College

London SW3 6LR, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Jadwiga A Wedzicha, MD

Sponsor contact

CONTACT

2075947947 j.wedzicha@imperial.ac.uk

Gavin C Donaldson, PhD

Sponsor contact

CONTACT

207 4947859 gavin.donaldson@imperial.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2022-06