Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06144476

Study of Inflammatory and Physiological Profiles of Healthy and Diseased Lung

Led by Guy's and St Thomas' NHS Foundation Trust · Updated on 2026-06-04

230

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

G

Guy's and St Thomas' NHS Foundation Trust

Lead Sponsor

K

King's College London

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the immune patterns in the respiratory system to better understand the immune-related causes of common lung diseases like asthma and chronic obstructive pulmonary disease (COPD). This study includes people diagnosed or suspected to have airway disease, as well as healthy volunteers, to compare inflammatory and physiological profiles. The study is observational and focuses on identifying immune signatures throughout the lungs and circulation that relate to these airway conditions. Participants will be invited to join at key clinical moments such as treatment changes or disease flare-ups and may attend optional bronchoscopy visits to collect lung samples. The study involves yearly visits, with additional visits during disease exacerbations or treatment adjustments. Procedures include questionnaires, lung function tests (spirometry or oscillometry), sputum and nasal sample collection, exhaled breath analysis, blood draws, and optionally, bronchoscopy to collect lung tissue and fluid samples. During the study, participants will undergo various assessments including disease-specific questionnaires, lung tests, and biological sample collection at King's College London and Guys and St Thomas' NHS Foundation Trust. Researchers will analyze blood samples over six years to identify immune types related to airway diseases and monitor their stability. The study tracks participants annually and at times of clinical changes, with safety and data collection monitored throughout the observation period.

CONDITIONS

Brief Title

Study of Inflammatory and Physiological Profiles of Healthy and Diseased Lung

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participant is willing and able to give informed consent for participation in the study
  • Aged 18 years or above
  • Patient with known or suspected airway disease
  • Healthy volunteer considered to be in good health with no significant comorbidity such as immune disorder or cancer
Not Eligible

You will not qualify if you...

  • Known or suspected current pulmonary tuberculosis, HIV, Hepatitis B, or Hepatitis C
  • Surgery within the preceding 6 weeks
  • Participants who are pregnant
  • History of psychiatric, medical, or surgical disorders that may interfere with participation or study completion
  • Alcohol or recreational drug abuse
  • Diagnosis of immunodeficiency requiring treatment
  • Unable to provide written informed consent
  • Unable to read or write English
  • Considered an unsuitable candidate for the study by the investigator

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - Up to 6 years

Participants are invited for research visits at clinically relevant time points such as treatment changes or disease exacerbations, and yearly visits to assess their lung health and collect samples.

Yearly visits and additional visits at clinically relevant time points

Optional Diagnostic Evaluation

Duration - Up to 6 years

Participants may choose to undergo optional bronchoscopy procedures to collect lung samples for detailed analysis, repeated once per year or at times of clinical changes.

Optional bronchoscopy visits occurring within the study centers

Trial Site Locations

Total: 1 location

1

Guy's & St Thomas' NHS Foundation Trust

London, London, United Kingdom, SE1 9RT

Actively Recruiting

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Research Team

G

Gillian Radcliffe, MRes

S

Steven Cass, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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