Skip to main content
Clinical Trials/ISRCTN15785949
ISRCTN15785949
Active, not recruiting
未知

Risk stratification of interstitial lung abnormalities using hyperpolarised xenon MRI and blood biomarkers

Oxford University Hospitals NHS Trust0 sites60 target enrollmentAugust 27, 2024

Overview

Phase
未知
Intervention
Not specified
Conditions
The progression of interstitial lung abnormalities into interstitial lung disease
Sponsor
Oxford University Hospitals NHS Trust
Enrollment
60
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 27, 2024
End Date
June 1, 2029
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.Participant is willing and able to give informed consent for participation in the study.
  • 2\.Male or Female, aged over 18 and under 85 years of age
  • 3\.Investigators are of the opinion that the participant is able and willing to comply with the study requirements
  • 3\.1\.Lung function tests that are normal or near normal – FVC and TLCO \>70% predicted for age and gender
  • 3\.2\.CT imaging fulfils criteria for ILA –
  • 3\.2\.1\.Incidental identification of non\-dependent abnormalities on Chest CT, including ground glass or reticular abnormalities, lung distortion, traction bronchiectasis and honeycombing
  • 3\.2\.2\.Occupying up to 10% of the lung as agreed independently by two consultant thoracic radiologists

Exclusion Criteria

  • 1\.Unable to provide informed consent
  • 2\.Contraindication to MRI e.g. shrapnel injury, heavily tattooed, severe claustrophobia
  • 3\.Any significant disease or disorder which, in the opinion of the investigator, might influence the interpretation of the clinical data e.g. Significant co\-pathology (e.g. emphysema, poorly controlled asthma, heart failure, pulmonary thromboembolic disease, Covid\-19 condition, pneumotoxic agents resulting in lung damage)
  • 4\.Clinical frailty score of 6 or above
  • 5\.Female participant who is pregnant, lactating or planning pregnancy.

Outcomes

Primary Outcomes

Not specified

Similar Trials