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Diffuse Parenchymal Lung Disease clinical trials

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NCT ID: NCT06171425 Not yet recruiting - Frailty Clinical Trials

Evaluation of Patients With Diffuse Parenchymal Lung Diseases Regarding Frailty

Start date: December 25, 2023
Phase:
Study type: Observational

There are very few studies in the literature examining the frailty levels of diffuse parenchymal lung disease (DPLD) patients and its effect on their functional status despite the high prevalance of frailty in patients with DPLD This observational study aims to learn about the relationship between frailty and functional capacity and balance in DPLD patients compared to healthy subjects.

NCT ID: NCT04392726 Recruiting - Clinical trials for Diffuse Parenchymal Lung Disease

Ultra-Low Dose Computed Tomography For Diagnosis And Follow-Up Of Patients With Diffuse Parenchymal Lung Disease (DPLD)

Start date: August 1, 2020
Phase:
Study type: Observational

The primary intention of this study is to determine the diagnostic performance of ultra-low-dose CT (ULDCT) in diagnosis and follow-up of diffuse parenchymal lung disease (DPLD). We hypothesize that inspiratory and expiratory chest ULDCT has comparable diagnostic yield to standard dose chest High-resolution computed tomography (HRCT) and utility for follow-up of patients with known DPLD. We will study this hypothesis through the following aims: 1. Determine whether inspiratory and expiratory ULDCT are comparable to HRCT in identifying mosaic attenuation due to air-trapping. 2. Determine whether ULDCT is as good as HRCT for follow-up of patients with established DPLD to identify disease progression.

NCT ID: NCT03101397 Active, not recruiting - Clinical trials for Diffuse Parenchymal Lung Disease

The Clinical Value of Serum KL-6 Changes on Evaluating Disease Development in Different Diffuse Parenchymal Lung Disease

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

Diffuse Parenchymal Lung Disease(DPLD) is a chronic progressive fibrosis lung disease that with a highly variable clinical process.Krebs von den Lungen-6 (KL-6) is a high-molecular-weight glycoprotein, classified as human MUC1 mucin, that is produced mainly by regenerating type II pneumocytes.Serum levels of KL-6 have been shown to be elevated in patients with DPLD and could predict progress, but unaware of the differential threshold. The objective of this study was to perspectively and sequentially monitor serum KL-6 levels in patients with different DPLD,then analyze its clinical value and find the differential threshold.

NCT ID: NCT02615938 Suspended - Clinical trials for Interstitial Lung Disease

Hydroxychloroquin (HCQ) in Pediatric Interstitial Lung Disease (ILD)

HCQ-chILD-EU
Start date: April 2015
Phase: Phase 2
Study type: Interventional

This is an exploratory Phase 2a, randomized, double-blind, placebo-controlled, parallel-group, multinational study investigating the initiation or withdrawal of hydroxychloroquine in subjects with chILD.

NCT ID: NCT01948518 Completed - Clinical trials for Pulmonary Hypertension

Effect of Sildenafil on Diffusion Capacity in Patients With PH and Parenchymal Lung Disease

Start date: June 2009
Phase: N/A
Study type: Interventional

The purpose of this study was to investigate the acute effects of sildenafil on diffusion capacity, a commonly performed pulmonary function test, which is used to assess the lungs' gas exchange capability. This study does not assess safety or efficacy of the drug. The study does not have clinical end points. The variables studied are diffusion capacity and 6 minute walk after a single dose of sildenafil. This study has been completed.

NCT ID: NCT01462006 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Double-blind Placebo-controlled Pilot Study of Sirolimus in Idiopathic Pulmonary Fibrosis (IPF)

Start date: October 2011
Phase: N/A
Study type: Interventional

Idiopathic pulmonary fibrosis (IPF) is an illness characterized by progressive decline in lung function and premature death from respiratory failure. Fibrocytes are a novel population of bone marrow-derived circulating progenitor cells that have been shown to traffic to the lungs and contribute to fibrosis in animal models of pulmonary fibrosis, and whose numbers correlate with the degree of fibrosis and with survival in human pulmonary fibrosis. The investigators propose to test the hypothesis that therapy with the mTOR inhibitor, sirolimus, reduces the number of circulating fibrocytes in patients with IPF. The investigators propose to test this hypothesis in short-term pilot trial of sirolimus in patients with IPF to determine its effect on the number and phenotype of circulating fibrocytes.

NCT ID: NCT00453713 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Race, Ethnicity, and Diffuse Parenchymal Lung Disease

Start date: July 2006
Phase: N/A
Study type: Observational

The purpose of this study is to identify factors that contribute to higher mortality rates among blacks and Hispanics with diffuse parenchymal lung disease.