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Interstitial Lung Disease clinical trials

View clinical trials related to Interstitial Lung Disease.

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NCT ID: NCT05986318 Not yet recruiting - Lung Cancer Clinical Trials

Reducing Respiratory Symptoms of Pulmonary Irradiation in Interstitial Lung Disease

RESPIRE-ILD
Start date: May 1, 2024
Phase: Phase 2
Study type: Interventional

In this double-blind phase II randomized controlled trial, patients with lung cancer or ≤2 oligometastatic pulmonary lesions and a concomitant diagnosis of ILD who are planned for radical Radiation Therapy (RT) will be randomized using a 2 x 2 factorial design to oral N-acetylcysteine (NAC) versus placebo, and also to short course corticosteroids versus placebo.

NCT ID: NCT05947422 Not yet recruiting - Clinical trials for Interstitial Lung Disease

CT Quantitative Assessment of Interstitial Lung Disease

Start date: August 1, 2023
Phase:
Study type: Observational [Patient Registry]

Interstitial lung disease (ILD) refers to a broad category of heterogeneous lung diseases with different etiologies and features characterized by inflammation and fibrosis of the lung parenchyma and manifested as exertional dyspnea, interstitial patterns on high resolution computed tomography (HRCT), and abnormal pulmonary function tests (PFTs) The aim of this study is to investigate is there any correlation between changes seen in the lung parenchyma by HRCT and the pulmonary functions of the patients.

NCT ID: NCT05785065 Not yet recruiting - Systemic Sclerosis Clinical Trials

Mycophenolate Mofetil in Systemic Sclerosis With Subclinical Interstitial Lung Disease

SSc-mILD
Start date: December 2023
Phase: Phase 2
Study type: Interventional

The goal of this pilot study is to assess the feasibility of a larger study on the efficacy of mycophenolate mofetil in people diagnosed with systemic sclerosis with mild lung involvement. Participants will be recruited over 12 months at 3 academic centers and assigned randomly to receive either mycophenolate mofetil or placebo, a look-alike substance that contains no active drug, for 96 weeks.

NCT ID: NCT04897048 Not yet recruiting - Clinical trials for Interstitial Lung Disease

Effect of Short-term Oxygen During CPET in ILD

Start date: July 1, 2023
Phase: N/A
Study type: Interventional

In a randomized, sham-controlled crossover trial the investigators will test whether supplemental oxygen given during cardiopulmonary exercise testing will improve exercise performance and physiological parameters in patients with interstitial lung disease.

NCT ID: NCT04719078 Not yet recruiting - Lung Diseases Clinical Trials

Thorax MRI for Evaluation of Lung Morphology, Ventilation and Perfusion

Start date: June 1, 2023
Phase: N/A
Study type: Interventional

In spite of the considerable technical difficulties, several publications confirm the potential that T1-maps and MRI to characterize pathological changes in lung tissue. However, existing literature still cannot provide a final evaluation of the presented methods. Study participants won't have any disadvantage in participating the study since all of them undergo next to the MRI-Scan also the two standard methods: CT and lung function test. In this study the value of chest MR compared to CT and LFT in the evaluation of morphological lung changes and their correlation to lung ventilation and perfusion will be evaluated.

NCT ID: NCT04532346 Not yet recruiting - Clinical trials for Interstitial Lung Disease

Hydroxychloroquine in Children's Interstitial Lung Diseases With Genetic Causes

Start date: March 2024
Phase: Early Phase 1
Study type: Interventional

The aim of this proposed study is to evaluate the efficacy and safety of hydroxychloroquine (HCQ) in children's interstitial lung diseases(chILD) with genetic causes. This study is a randomized controlled clinical trial.

NCT ID: NCT04193592 Not yet recruiting - Clinical trials for Interstitial Lung Disease

Efficacy and Safety of Pirfenidone Treatment in HPS-ILD

PEARL
Start date: December 1, 2019
Phase: Phase 2
Study type: Interventional

This research study will explore the safety and efficacy of the drug, pirfenidone, in patients with a diagnosis of Hermansky-Pudlak Syndrome (HPS) who have an associated interstitial lung disease (ILD) over a planned period of 56 weeks.

NCT ID: NCT04089826 Not yet recruiting - Clinical trials for Interstitial Lung Disease

Long Term Oxygen Therapy in Patients With Interstitial Lung Disease

Start date: September 2019
Phase:
Study type: Observational

Study the effect of using long term oxygen therapy in patients with interstitial lung disease and chronic hypoxia

NCT ID: NCT03958162 Not yet recruiting - Clinical trials for Interstitial Lung Disease

The Comparison of Uniportal and Tubeless Video Assisted Thoracic Surgery and Transbronchial Lung Cryobiopsy in the Diagnosis of Interstitial Lung Disease

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

To compariing the uniportal and tubeless video assisted thoracic surgery and trnsbronchial lung cryobiopsy within the multidisciplinary discussion context in the diagnosis of interstitial lung disease,and assess the safety and cost-effectiveness. This is a prospective control trial.

NCT ID: NCT03870828 Not yet recruiting - Clinical trials for Interstitial Lung Disease

Clinical Characteristics of Interstitial Pneumonia With Autoimmune Features (IPAF) - a Multicenter Prospective Study

Start date: March 18, 2019
Phase:
Study type: Observational

Interstitial pneumonia with autoimmune features (IPAF) was defined in 2015 by the Working Group of the European Respiratory Society (ERS) and the American Thoracic Society (ATS) as interstitial pneumonia with some clinical and/or serological features suggesting presence of an underlying autoimmune disorder. However, ofiicial criteria for diagnosis of an autoimmune disease are not met. Aims of the study: 1. Determine the incindence of IPAF in comparison with interstitial lung diseases (ILDs) and classic autoimmune diseases (ADs) in polish pulmonological centers. 2. Clinical, serological, functional and radiological and histopathological characteristics of IPAF patients. 3. Analysis of diagnostic strategies towards specific IPAF subgroups. 4. Characterictics of potencial diagnostic, predictive and prognostic features of IPAF. 5. Prospective assessment of IPAF patients in the courseof 5 years in order to determine stability of the diagnosis and potential progression to other diseases, e.g. ADs.