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Pulmonary Fibrosis clinical trials

View clinical trials related to Pulmonary Fibrosis.

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NCT ID: NCT02370693 Completed - Systemic Sclerosis Clinical Trials

Comparing and Combining Bortezomib and Mycophenolate in SSc Pulmonary Fibrosis

Start date: March 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to look at whether bortezomib, mycophenolate or the combination of both is better to treat scarring of the lung caused by Systemic Sclerosis.

NCT ID: NCT02368340 Completed - Clinical trials for Hermansky Pudlak Syndrome

A Longitudinal Study of Hermansky-Pudlak Syndrome Pulmonary Fibrosis

Start date: March 2015
Phase:
Study type: Observational

Hermansky-Pudlak Syndrome (HPS) is a rare genetic disease that is associated with oculocutaneous albinism, bleeding, granulomatous colitis, and pulmonary fibrosis in some subtypes, including HPS-1, HPS-2, and HPS-4. Pulmonary fibrosis causes shortness of breath and progressive decline in lung function. In HPS patients with at-risk subtypes, almost all adults eventually develop fatal pulmonary fibrosis unless they undergo lung transplantation. The purpose of this study is to identify the earliest measurable pulmonary disease activity in individuals at-risk for HPS pulmonary fibrosis. The study also aims to develop biomarkers that will aid in understanding of the causes of HPS pulmonary fibrosis and facilitate more rapid conduct of therapeutic trials in HPS patients with mild pulmonary disease in the future.

NCT ID: NCT02345070 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Efficacy and Safety of SAR156597 in the Treatment of Idiopathic Pulmonary Fibrosis

ESTAIR
Start date: May 1, 2015
Phase: Phase 2
Study type: Interventional

Primary Objective: To evaluate, in comparison with placebo, the efficacy of 2 dose levels/regimens of SAR156597 administered subcutaneously during 52 weeks on lung function of participants with Idiopathic Pulmonary Fibrosis (IPF). Secondary Objectives: To evaluate the efficacy of 2 dose levels/regimens of SAR156597 compared to placebo on IPF disease progression. To evaluate the safety of 2 dose levels/regimens of SAR156597 compared to placebo in participants with IPF.

NCT ID: NCT02315586 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Characterization of Apolipoprotein A-I Pathways in Idiopathic Pulmonary Fibrosis

Start date: January 28, 2015
Phase:
Study type: Observational

Background: - Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease that becomes worse over time. There is currently no effective treatment for it. Researchers want to study the disease and learn new ways to treat it. Objectives: - To discover new pathways that are involved in pulmonary fibrosis. To develop new drugs that may be used to treat pulmonary fibrosis. Eligibility: - People at least 18 years old with IPF. - Healthy volunteers at least 18 years old. Design: - Participants will be screened with medical history, questionnaire, and physical exam. They will have blood, lung, and walking tests and chest scans. - All participants will have 1 study visit, including: - Medical history and physical exam. - Questions about their breathing. - Blood tests. - Breathing tests. - Six-minute walk test. - Pregnancy test. - Chest x-ray (healthy volunteers) or chest CT scan (people with pulmonary fibrosis ). - Small area of skin may be removed. - Genetic tests of blood and skin samples. Participants will probably not be informed of any findings. Samples may be used to make stem cells for use in research. Participants may be contacted in the future to give consent for this research. - Some participants will have repeat visits over many years, repeating many of the study tests.

NCT ID: NCT02277145 Completed - Clinical trials for Post-radiotherapy Pulmonary Fibrosis

A Study on Radiation-induced Pulmonary Fibrosis Treated With Clinical Grade Umbilical Cord Mesenchymal Stem Cells

Start date: October 2014
Phase: Phase 1
Study type: Interventional

Radiation therapy is one of the main means for treating malignant tumor, during which radioactive lung injury is inevitable. Currently there is nearly no effective clinical treatment for late post-radiotherapy pulmonary fibrosis. This study intends to carry out an open, single-center, non-randomized phase I clinical trial. During the treatment, the local lesions will be fully lavaged, and then clinical grade umbilical cord mesenchymal stem cells (MSCs) will be injected directly into the lesion by fiberoptic bronchoscopy. After six-month observation, the investigators will initially evaluate the safety and effectiveness of the treatment by measuring two key indicators-the CT density histogram and the patients' self-evaluation, and one secondary indicator—the changes of TGF-β1 contents, both before and after the treatment. Meanwhile, the investigators will make a preliminary discuss about the possible immunomodulatory effects of the umbilical cord MSCs.

NCT ID: NCT02268981 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Effects of an Oxymizer® During Daytime in Patients With Pulmonary Fibrosis (IPF)

Start date: September 2014
Phase: N/A
Study type: Interventional

This study will investigate the effects of a reservoir nasal cannula (Oxymizer®) compared to a conventional nasal cannula (CNC) in patients with idiopathic pulmonary fibrosis.

NCT ID: NCT02267655 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

3 Part Study to Assess Inhaled Nitric Oxide on Functional Pulmonary Imaging in Subj. Pulmonary Hypertension Associated w/ COPD and IPF

Start date: May 2015
Phase: Phase 1
Study type: Interventional

The objective of this exploratory study is to examine the utility of high resolution computed tomography (HRCT) to measure changes in functional pulmonary imaging parameters as a function of short term a) iNO administration and b) nitric oxide (NO) cylinder concentration using the investigational medical device INOpulse® DS-C in subjects with WHO Group 3 PH associated with COPD on LTOT (Part 1) and in Subjects with WHO Group 3 PH associated with Idiopathic Pulmonary Fibrosis (IPF) on LTOT (Part 2 and Part 3)

NCT ID: NCT02257177 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

RCT (Randomized Control Trial) of TD139 vs Placebo in HV's (Human Volunteers) and IPF Patients

Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This study will be divided into 2 parts. Part 1 is a randomized, double-blind, single centre, placebo-controlled, single ascending dose (SAD) phase I study designed to assess the safety, tolerability, PK and PD (Pharmacodynamic) of TD139 in up to 36 healthy male subjects. Part 2 will be a randomized, double-blind, multi-centre, placebo-controlled, multiple dose expansion cohort, designed to assess the safety, tolerability, PK and PD of TD139 in up to 24 male subjects and female subjects of non child-bearing potential with IPF.

NCT ID: NCT02248064 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Auto-titrating Oxygen in Chronic Respiratory Failure

ASI1
Start date: July 2014
Phase: N/A
Study type: Interventional

Long term oxygen therapy (LTOT) increases the life span of patients with chronic obstructive pulmonary disease who have low oxygen levels. However, even when on oxygen therapy at home, from time to time patients still have low oxygen levels especially when walking which can be harmful. The investigators have designed a new system of delivering oxygen to overcome the above problem. The system measures the oxygen saturations of a patient and subsequently adjust the flow of oxygen to meet a pre-set oxygen saturation target. Hypothesis: the investigators intelligent oxygen therapy system is better at reducing low levels of oxygen during a 6 minute walk than usual ambulatory oxygen for patients with chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis.

NCT ID: NCT02188758 Completed - Cystic Fibrosis Clinical Trials

Biomarkers of Iron Homeostasis and Responses to Cystic Fibrosis Pulmonary Exacerbation (CFPE) Treatment

Start date: July 2014
Phase: N/A
Study type: Observational

The goal of this study is to identify chemical compounds in the blood and sputum (i.e., biomarkers) that are associated with objective measurements of health status in patients with cystic fibrosis (CF). This study builds upon observations that blood levels of hepcidin-25, a protein that regulates how the body uses and stores iron, vary during CF pulmonary exacerbation (CFPE).