Better Tests- Improving Diagnostic Accuracy and Prognostication in Interstitial Lung Diseases

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorUniversity of Dundee

About this trial

Patients with interstitial lung diseases (ILD) suffer significant delays in obtaining a diagnosis, and objective evidence of support for immunosuppressive therapies, due to weaknesses in the diagnostic tests available in ILD clinics.

This project will assess several non-invasive assessments, focusing on blood and breath based sampling, to identify candidate tests that may translate through to routine clinical use. The tests being assessed will be initially employed in Pigeon Fanciers, a group recognised to be at high risk of developing ILD compared to age matched controls, due to their regular exposure to a known cause of ILD. Candidate tests will also be assessed for change over time in this group. Tests which show promise will then be utilised in patients with ILD diagnoses, including those with severe respiratory failure, to assess their acceptability to patients and their ability to provide useful prognostic information, to allow powering of future definitive clinical trials.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Active Pigeon Fanciers, or patients with ILD presenting to clinics or hospital services with severe respiratory failure due to ILD

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

750 Participants
are grouped into 3 trial groups
Group A: Pigeon Fanciers
Group B: Clinic patients with ILD
Group C: Hospital patients with ILD

Trial outcomes

Primary outcomes

1

Prediction of subsequent clinical outcomes

The utilised tests will be examined for their ability to accurately predict the subsequent diagnostic label for ILD and clinical behaviour

Time frame
5 years
2

Acceptability to participants

The tests employed will be assessed for their ease of performance and acceptability from a participant perspective

Time frame
5 years

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Dundee

Lead sponsor

British Pigeon Fanciers Medical Research

Collaborator

NHS Tayside

Collaborator