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Lung Diseases, Interstitial clinical trials

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NCT ID: NCT01915511 Recruiting - Clinical trials for Idiopathic Pulmonary Fibrosis, Interstitial Lung Disease

Idiopathic Pulmonary Fibrosis and Interstitial Lung Disease Prospective Outcomes Registry

IPF/ILD-PRO
Start date: June 2014
Phase:
Study type: Observational [Patient Registry]

This registry will collect data on the strategies used to achieve a diagnosis of Idiopathic Pulmonary Fibrosis (IPF) and Chronic Fibrosing Interstitial Lung Disease with Progressive Phenotype (ILD) and the treatment and management efforts applied throughout study follow-up, clinical outcome events and patient reported outcome data. Blood samples will be collected periodically throughout the study for use in future research efforts. For participants with non-IPF, chronic fibrosing ILD with progressive phenotype, HRCT images will be collected throughout the study for use in future research efforts.

NCT ID: NCT01858259 Recruiting - Systemic Sclerosis Clinical Trials

Treatment and Prevention of Progression of Interstitial Lung Disease in Systemic Sclerosis

Start date: May 2013
Phase: N/A
Study type: Observational [Patient Registry]

Systemic sclerosis (SSc) is an orphan, multiorgan disease affecting the connective tissue of the skin and all internal organs. Interstitial lung disease is a frequent morbidity and mortality-driving manifestation in systemic sclerosis. This observational trial (OT) is part of the collaborative project "DeSScipher", one out of five OTs to decipher the optimal management of systemic sclerosis. Aim of this observational try is to identify: - The state of clinical practice in Europe for prevention and treatment of interstitial lung disease and its impact on lung function and disease progression - The potential predictors and confounders for response to therapy

NCT ID: NCT01809574 Recruiting - Clinical trials for Idiopathic Pulmonary Fibrosis

The Role of Rheumatological Evaluation in the Management of Patients With Interstitial Lung Disease

Start date: May 2013
Phase: N/A
Study type: Observational

We hypothesized that the multi-disciplinary assessment of interstitial lung disease patients would lead to a more accurate diagnosis and consequently alterations in treatment regimens that may lead to improved outcomes.

NCT ID: NCT01776398 Recruiting - Smoking Cessation Clinical Trials

Collection of Airway, Blood and/or Urine Specimens From Subjects for Research Studies

Start date: August 29, 2012
Phase:
Study type: Observational

The purpose of this study is to obtain biologic materials from the blood, airways and/or urine of normal individuals and individuals with lung disease. The normal are used to establish a set of normal ranges for various parameters. These provide control information when compared to individuals with various pulmonary diseases, and will help in understanding of the etiology and pathogenesis of various lung diseases. The underlying hypothesis is that the pathologic morphological changes in the airway epithelium must be preceded by changes in the gene expression pattern of the airway epithelium and potentially in macrophages.

NCT ID: NCT01600378 Recruiting - Clinical trials for Diffuse Parenchymal Lung Diseases

Prospective Data Collection of Patients With Diffuse Parenchymal Lung Diseases

Start date: May 2012
Phase:
Study type: Observational

The purpose of this study is to generate a prospective database of all patients evaluated for diffuse parenchymal lung diseases to provide much needed data on the various disease aetiologies, incidence and prevalence rates, clinical and radiological presentations, pathologic correlations, disease progression and response to treatment, and final outcomes in this group of patients in Singapore.

NCT ID: NCT01450644 Recruiting - Lung Disease Clinical Trials

Evaluation of the Hospital2Home Palliative Care Service for Patients With Advanced Progressive Lung Disease

H2H-ILD
Start date: October 2011
Phase: Phase 2
Study type: Interventional

The investigators hypothesise that H2H will result in improved symptom control and quality of life and may be more cost-effective than standard best practice. Interstitial Lung Disease (ILD) is a lung condition characterised by progressive scarring - known as fibrosis. This is especially seen in patients with idiopathic pulmonary fibrosis (IPF). There around 2,000 new patients diagnosed in the UK every year with a similar number of deaths. Fibrotic-ILD causes breathing to slowly deteriorate and as there is no cure, an estimated two-thirds of patients die within five years of diagnosis. Patients suffer from many symptoms including shortness of breath, cough, low mood and fatigue which are currently being poorly managed. In addition, these patients suffer a poor health related quality of life whilst dying from their disease. In the later stages of their disease, these patients often end up in hospital (see appendix 1a) when there is no proven or effective treatment. Many die there despite wishing to be looked after and die at home. These patients rarely receive palliative care which may help to improve their symptoms, quality of life, address end of life planning needs and prevent hospital admission. The Hospital2Home case conference conducted in the patient's home (or place of their choice) aims to address this. At the case conference involving the patient, their carers, a specialist nurse, and all the community health professionals, a care plan specific to the patient will be developed. Each health professional will be aware of their responsibility and duties. The investigators will look at whether this results in better symptom control and better quality of life for the patient and their carer. The investigators will also examine whether this prevents emergency hospital admission and allows patients to die in their preferred place. The investigators will compare patients who receive the service immediately with those who receive it after a delay.

NCT ID: NCT01280994 Recruiting - Clinical trials for Interstitial Lung Disease

Hyperpolarized 129Xe MRI for Imaging Pulmonary Function

Start date: January 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to develop and evaluate the usefulness of MRI using 129Xe gas for regional assessment of pulmonary function. Specifically, three forms of 129Xe MRI contrast will be the investigators focus - 1) imaging of the 129Xe ventilation distribution, 2) imaging the alveolar microstructure via the 129Xe apparent diffusion coefficient (ADC), and 3) imaging 129Xe that dissolves in the pulmonary blood and tissues upon inhalation. Such imaging of 129Xe gas transfer is expected to be uniquely sensitive to pathologies affecting gas exchange (fibrosis, emphysema, pulmonary hypertension) and provide new insights regarding the normal resting heterogeneity of pulmonary gas exchange.

NCT ID: NCT01211015 Recruiting - Clinical trials for Interstitial Lung Diseases

Endoplasmic Reticulum Stress in Chronic Respiratory Diseases

Start date: July 2010
Phase: N/A
Study type: Observational

Aim: To investigate whether ER stress is implicated in the pathogenesis of various pulmonary disorders Measurement: 1. Unfolded protein responses (UPRs) in blood (PBMCs)of patients 1. CHOP 2. GRP 78 and so on 2. Unfolded protein responses (UPRs) in blood (PBMCs)of healthy controls 1. CHOP 2. GRP 78 and so on

NCT ID: NCT01088217 Recruiting - Clinical trials for Idiopathic Pulmonary Fibrosis

Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF)

GWAS
Start date: July 2008
Phase:
Study type: Observational

The purpose of this study is to investigate inherited genetic factors that play a role in the development of familial pulmonary fibrosis and to identify a group of genes that predispose individuals to develop pulmonary fibrosis. Finding the genes that cause pulmonary fibrosis is the first step at developing better methods for early diagnosis and improved treatment for pulmonary fibrosis. The overall hypothesis is that inherited genetic factors predispose individuals to develop pulmonary fibrosis.

NCT ID: NCT00841750 Recruiting - Clinical trials for Lung Diseases, Interstitial

Chest Tube After a Video-assisted Thoracoscopic Surgery Pulmonary Wedge Resection

NOTUBE
Start date: July 2008
Phase: Phase 3
Study type: Interventional

After performing VATS pulmonary wedge resections, a chest tube is routinely left in the pleural cavity to drain possible air leaks and fluid accumulations. Chest tubes after VATS pulmonary wedge resections are left in place a minimum of 1 day. However, this practice has no scientific foundations. The investigators believe it is possible to avoid the placement of a chest tube after this procedure in a great amount of patients. This is a randomized controlled clinical trial with analysis blinding in which the investigators want to compare the outcomes between installing a chest tube or not after VATS pulmonary wedge resections. The investigators will include consecutively patients with interstitial lung disease or indeterminate pulmonary nodules undergoing this procedure, at the participating institutions. The investigators calculated a sample size of 50 subjects in each group using pneumothorax < 10% data from Luckraz et al and to determine a difference of hospital stay of 2 versus 1 day; DS(1.5), power = 0.9 and alpha = 0.05.