Prospective Study of Fibrosis In the Lung Endpoints (PROFILE - Central England)
NCT01134822 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 330
Last updated 2018-10-15
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.
Conditions
Sponsors & Collaborators
- collaborator OTHER_GOV
- collaborator INDUSTRY
-
CRAFT Consortium
collaborator UNKNOWN - collaborator OTHER
-
University of Nottingham
lead OTHER
Principal Investigators
-
Gisli Jenkins, Dr · University of Nottingham
-
Robert Berg, Dr · University Hospitals of Derby and Burton NHS Foundation Trust
-
Sanjay Agarwal, Dr · University Hospitals, Leicester
-
Moira White, Dr · Sheffield Teaching Hospitals NHS Foundation Trust
-
Khaled Amsha, Dr · Sherwood Forest Hospitals NHS Trust
-
David Thickett, Dr · University Hospital Birmingham NHS Foundation Trust
-
Uttam Nanda, Dr · Burton Hospitals NHS Foundation Trust
Eligibility
- Min Age
- 18 Years
- Max Age
- 85 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-07-31
- Primary Completion
- 2017-09-05
- Completion
- 2017-09-05
Countries
- United Kingdom
Study Locations
More Related Trials
-
Genomic and Proteomic Analysis of Disease Progression in Idiopathic Pulmonary Fibrosis (IPF)
NCT00373841 ·Status: RECRUITING
-
Evaluation of Patients With Idiopathic Pulmonary Fibrosis (IPF) Through an IPF Registry
NCT00212511 ·Status: WITHDRAWN
-
Prospective Evaluation of Biomarker Profiles in Idiopathic Pulmonary Fibrosis
NCT02151435 ·Status: COMPLETED
-
A Pilot Study to Assess Body Mass Composition Measurement Using BIA and Muscle Ultrasound in IPF and PPF Patients on Anti-fibrotic Medications
NCT07332117 ·Status: RECRUITING
-
Assessment of Peripheral Endothelial Function in Idiopathic Pulmonary Fibrosis
NCT02594059 ·Status: COMPLETED ·Phase: NA
-
Functional and Structural Lung Imaging in Chronic Obstructive Pulmonary Disease
NCT04966221 ·Status: UNKNOWN
-
Impulse Oscillometry for Prognostication in Idiopathic Pulmonary Fibrosis
NCT03898284 ·Status: COMPLETED
-
Investigating Trends in Quality of Life in Patients With Idiopathic Pulmonary Fibrosis (IPF) Under Treatment With Nintedanib
NCT03710824 ·Status: COMPLETED
-
Exhaled Breath Condensate Biomarkers and Cough in IPF
NCT02630940 ·Status: COMPLETED
-
Investigating Idiopathic Pulmonary Fibrosis in Greece
NCT03074149 ·Status: COMPLETED
-
A Study to Characterize the Disease Behavior of Idiopathic Pulmonary Fibrosis (IPF) and Interstitial Lung Disease (ILD) During the Peri-Diagnostic Period
NCT03261037 ·Status: COMPLETED ·Phase: NA
-
Characterization of Apolipoprotein A-I Pathways in Idiopathic Pulmonary Fibrosis
NCT02315586 ·Status: COMPLETED
-
Advancing Prevention of Pulmonary Fibrosis
NCT04564183 ·Status: ACTIVE_NOT_RECRUITING
-
Optimising Screening for Early Disease Detection in Familial Pulmonary Fibrosis
NCT05367349 ·Status: UNKNOWN
-
Expanded Access Program of Nintedanib in Patients With Idiopathic Pulmonary Fibrosis
NCT02230982 ·Status: NO_LONGER_AVAILABLE
-
Study on Phenotypic Characterization of Combined Pulmonary Fibrosis and Emphysema
NCT01121367 ·Status: COMPLETED
-
Idiopathic Pulmonary Fibrosis and Interstitial Lung Disease Prospective Outcomes Registry
NCT01915511 ·Status: RECRUITING
-
Biomarker Discovery for Novel Drug Development in Idiopathic Pulmonary Fibrosis
NCT01718990 ·Status: COMPLETED
-
Development of Airway Absorption Sampling Methods
NCT04494334 ·Status: WITHDRAWN
-
Precision Diagnosis and Care for Families With Pulmonary Fibrosis in Ireland
NCT06702228 ·Status: RECRUITING
-
Microarray Analysis of Gene Expression in Idiopathic Pulmonary Fibrosis (IPF)
NCT00258544 ·Status: ACTIVE_NOT_RECRUITING
-
PRospective phenotypIng and Multi-omic Endotyping of Progressive Pulmonary Fibrosis
NCT06855329 ·Status: RECRUITING
-
It's Not JUST Idiopathic Pulmonary Fibrosis Study
NCT03670576 ·Status: UNKNOWN
-
Correlation Between Changes in Lung Function and Changes in Cough and Dyspnoea in Nintedanib-treated Connective Tissue Disease Interstitial Lung Disease (CTD-ILD) Patients
NCT05503030 ·Status: ACTIVE_NOT_RECRUITING
-
Role of the Fibroblast Activation Protein (FAP) as Biomarker of Fibrotic Lung Diseases
NCT06189820 ·Status: RECRUITING ·Phase: PHASE2