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Clinical Trials/NCT01134822
NCT01134822
Completed
Not Applicable

Prospective Study of Fibrosis In the Lung Endpoints (PROFILE - Central England)

University of Nottingham1 site in 1 country330 target enrollmentJuly 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Idiopathic Pulmonary Fibrosis
Sponsor
University of Nottingham
Enrollment
330
Locations
1
Primary Endpoint
Discover biomarkers in IPF
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The overall aim of this study is to develop a test that predicts the prognosis of IPF (Idiopathic Pulmonary Fibrosis) and which could be used to determine whether new treatments for IPF are likely to work.

Detailed Description

The overall objectives of this study are * Discover and validate novel biomarkers and gene expression profiles for use in subsequent intervention studies in patients with IPF * To prospectively validate a panel of previously published biomarkers in patients with well characterized idiopathic fibrosing lung disease * Investigate genetic associations and epigenetic modifications which affect disease severity and progression * Prospectively evaluate longitudinal disease behaviour in patients with IPF and NSIP with a view to developing composite clinical end-points for subsequent use in intervention studies in patients with IPF Biomarkers that can be used for the following purposes will be identified: * Identify patients (Diagnostic)(e.g. discriminate between health and disease) * Correlate with disease severity (extent of disease, staging of disease) * Predict clinical progression (Prognostic)(stable vs progressive disease) * Track response to therapy (Therapeutic response)- Predict response to known efficacious treatments \& Correlates with changes in clinical endpoints/mortality/quality of life * Predict risk of exacerbations (could be used to prevent exacerbations or reduce their severity) * Correlate with complications and/or comorbidities (e.g. biomarkers of Pulmonary Arterial Hypertension, Gastro Oesophageal Reflux in IPF, etc)

Registry
clinicaltrials.gov
Start Date
July 2010
End Date
September 5, 2017
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • A diagnosis of IPF using the consensus criteria (32)and Non Specific Interstitial Pneumonia.
  • Between the age group 18-85 years.
  • Sub classified into Mild (TLCO\>60), Moderate (TLCO 40-60), Severe (TLCO\<40).
  • People who volunteer to undergo a bronchoscopy for research

Exclusion Criteria

  • People who do not have IPF/NSIP (i.e. Hypersensitivity Pneumonitis, Sarcoidosis)
  • People who cannot give informed consent.
  • People who are being considered for bronchoscopy, any contra-indication to undergoing this procedure as set out in the British Thoracic Society guidelines (Thorax 2001; 56: suppl I: i1-i21). These will be part of the study but not undergo the Broncho Alveolar Lavage.

Outcomes

Primary Outcomes

Discover biomarkers in IPF

Time Frame: 36 months

* Discover and validate novel biomarkers for use in subsequent intervention studies in patients with IPF * To prospectively validate a panel of previously published biomarkers in patients with well characterized idiopathic fibrosing lung disease * Investigate genetic associations and epigenetic modifications which affect disease severity and progression

Secondary Outcomes

  • Survival from Pulmonary fibrosis.(10 years)

Study Sites (1)

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