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Lung Diseases, Interstitial clinical trials

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NCT ID: NCT05445817 Recruiting - Clinical trials for Interstitial Lung Disease

Pulmonary Care and Research Collaborative Patient Registry

Start date: July 2022
Phase:
Study type: Observational [Patient Registry]

The purpose of this research study is to build and maintain a registry of people with interstitial lung disease (ILD). Medical information collected for this registry may be used to advance ILD and pulmonary research and improve patient care. This is an observational registry. Participants will not receive any investigational treatments or investigational drugs as part of their participation in this registry.

NCT ID: NCT05417776 Recruiting - Clinical trials for Interstitial Lung Disease

Collagen-targeted PET Imaging for Early Interstitial Lung Disease

Start date: September 28, 2022
Phase: Phase 2
Study type: Interventional

The goal of this study is to investigate the ability of [68Ga]CBP8 to detect collagen deposition in early interstitial lung disease.

NCT ID: NCT05396469 Completed - Clinical trials for Lung Diseases, Interstitial

Using Thoracic Ultrasound to Detect Interstitial Lung Disease in Patients With Rheumatoid Arthritis

AURORA
Start date: June 10, 2022
Phase:
Study type: Observational

Background: Pulmonary diseases are significant contributors to morbidity and mortality in patients with rheumatoid arthritis (RA). One of the most common pulmonary manifestation in RA is interstitial lung disease (RA-ILD). Consequently, RA-ILD may be prevalent in approximately 30% and clinically evident in about 10% of RA patients. Since the median survival for patients with manifest RA-ILD is only 6.6 years, feasible methods of detecting early RA-ILD are warranted. Objectives: To determine the diagnostic accuracy of thoracic ultrasound (TUS), using a 14-zone protocol, for ILD in RA patients with respiratory symptoms by using chest high-resolution computed tomography (HRCT) as the reference standard. The secondary aim is to evaluate the diagnostic accuracy for the blood biomarkers surfactant protein-D (SP-D) and microfibrillar-associated protein 4 (MFAP4) in the detection of ILD in this group of patients. Data collection: Participants will be included after signing the informed consent; data will be collected and stored in a REDCap database. Eligibility criteria for participants and settings where data will be collected: Patients eligible for inclusion are consenting adults (≥18 years) diagnosed with RA (according to the 2010 ACR-criteria for RA) and respiratory symptoms indicating RA-ILD, based on the presence of at least one of the following symptoms: unexplained dyspnoea, unexplained cough and/or a residual pneumonia or a chest X-ray indicating interstitial abnormalities in the lung. Whether participants form a consecutive, random or convenience series: Participants form a consecutive series of up to 80 individuals in total. Description of the index test and reference standard: Patients suspected of having RA-ILD will undergo a 14 zone TUS as index test performed by a junior resident in rheumatology, who is certified by the European Respiratory Society in performing TUS assessment. The anonymised images will be stored, and scored by the junior resident and two senior rheumatologists, who have also received training in TUS, as well as a TUS and ILD experienced pulmonologist. Chest HRCT will be the gold standard, i.e. the ILD reference standard. Estimates of diagnostic accuracy and their precision: The two basic measures for quantifying the diagnostic accuracy of the TUS (index) test are the sensitivity and specificity in comparison to the chest HRCT. Statistical tests will be conducted using the McNemar test for correlated proportions.

NCT ID: NCT05392881 Recruiting - Clinical trials for Idiopathic Pulmonary Fibrosis

Interstitial Lung Disease Research Unit Biobank

ILDRU
Start date: August 9, 2021
Phase:
Study type: Observational [Patient Registry]

Establish a interstitial lung disease (ILD) registry and biorepository to lead towards a further understanding of the disease.

NCT ID: NCT05391100 Recruiting - Clinical trials for Rheumatoid Arthritis

Screening of Patients With Rheumatoid Arthritis for Interstitial Lung Disease

Start date: February 1, 2022
Phase:
Study type: Observational

The quantitative and qualitative analysis of RA lung involvement in the Hungarian population

NCT ID: NCT05382572 Recruiting - Clinical trials for Idiopathic Pulmonary Fibrosis

Pulmonary Fibrosis Foundation Community Registry

Start date: July 11, 2022
Phase:
Study type: Observational [Patient Registry]

Pulmonary fibrosis (PF) results from a diverse group of health conditions and affects the lives of patients (including those who are post lung transplant), caregivers and family members. The Pulmonary Fibrosis Foundation Community Registry will offer an online portal where participants can self-enroll and directly contribute information about their experience with PF to be compiled into a longitudinal data set for use by researchers.

NCT ID: NCT05375435 Recruiting - Clinical trials for Interstitial Lung Disease

Efficacy and Safety of Triple Therapy in Patients With Anti-MDA5 Antibody-positive Dermatomyositis

Start date: January 1, 2022
Phase: Phase 4
Study type: Interventional

We conduct this study to investigate the efficacy of triple therapy (high-dose glucocorticoids + cyclophosphamide + calcineurin inhibitor) compared with dual-therapy regimens (high-dose glucocorticoids + cyclophosphamide/calcineurin inhibitor) and whether it reduces the risk of poor pulmonary prognosis in patients with moderate to high risk anti-MDA5+ DM.

NCT ID: NCT05372926 Recruiting - Clinical trials for Interstitial Lung Disease

Physiological Effects of HFNC During Exercise in Patients With Fibrosing Interstitial Lung Diseases

HighFlowMusc
Start date: November 22, 2022
Phase: N/A
Study type: Interventional

in this study, the investigators aim to describe the effects of highflow nasal canulae oxygen therapy (HFNC) on respiratory muscle function during exercise in patients with fibrosing interstitial lung diseases (ILD) during an endurance test

NCT ID: NCT05365802 Recruiting - Clinical trials for Interstitial Lung Disease

FAPI PET for Lung Fibrosis

FAPI ILD
Start date: November 16, 2021
Phase: Early Phase 1
Study type: Interventional

This is a prospective exploratory biodistribution study in patients with interstitial lung disease (ILD). The purpose of this research study is to determine where and to which degree the FAPI tracer (68Ga-FAPI-46) accumulates in normal and fibrotic lung tissues of patients with interstitial lung disease. The study will include patients with interstitial lung disease who have or will initiate a new ILD medication OR will undergo tissue biopsy or surgery of the lung. The study will include 30 patients, the upper limit for PET imaging studies conducted under the Radioactive Drug Research Committee (RDRC) purview. Participants will be injected with up to 7 mCi of 68-GaFAPi and will undergo one PET/CT scan and one High Resolution CT of the lungs. The study is sponsored by Ahmanson Translational Theranostic Division at UCLA.

NCT ID: NCT05365009 Recruiting - Clinical trials for Interstitial Lung Disease Due to Systemic Disease

Registry of Autoimmune Interstitial Lung Disease

EPIMAR
Start date: April 10, 2022
Phase:
Study type: Observational [Patient Registry]

Interstitial lung diseases (ILD) constitute a group of entities characterized by inflammation and/or fibrosis of the lung parenchyma. In recent years, with the advent of new diagnostic tools and therapeutic options, multidisciplinary evaluation is essential, since it optimizes the interpretation of each case and the quality of care for these pathologies Consensus for the identification and management of ILD associated with SSc (ILD-SSc) is the only guideline published at present. In the others autoimmune ILD (Ai-ILD), screening, diagnosis, treatment and follow-up strategies are usually performed according to the criteria of the treating medical team. Guidelines regarding the follow-up and indication of immunosuppressive and antifibrotic treatment are lacking. Many questions on the horizon of the Ai-ILD should be answered as better quality evidence emerges from studies with a greater number of patients and better methodological design.