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Lung Diseases clinical trials

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NCT ID: NCT04925375 Recruiting - Clinical trials for Interstitial Lung Disease

Abatacept for the Treatment of Common Variable Immunodeficiency With Interstitial Lung Disease

ABCVILD
Start date: July 14, 2021
Phase: Phase 2
Study type: Interventional

There is no standard of care therapy for patients with granulomatous-lymphocytic interstitial lung disease (GLILD) seen in common variable immunodeficiency (CVID). Abatacept has recently looked promising for the treatment of patients with complex CVID. This study is a multi-site, phase II, randomized, blinded/placebo-controlled clinical trial in pediatric and adult subjects to determine the efficacy of abatacept compared to placebo for treatment of subjects with GLILD in the context of CVID. Funding Source - FDA OOPD

NCT ID: NCT04924465 Not yet recruiting - Clinical trials for Antisynthetase Syndrome

Evaluation of Interstitial Lung Disease Severity in Patients With Antisynthetase Syndrome According to Specific Autoantibodies Profile

TYPASS
Start date: June 2021
Phase:
Study type: Observational

Antisynthetase syndrome (ASS) is an overlap connective tissue disease characterized by the presence of myositis-specific autoantibodies directed against tRNA-synthetases. Clinical manifestations are myositis, interstitial lung disease (ILD), Raynaud's phenomenon, mechanic's hands and polyarthritis. Clinical presentation varies between ASS patients. ASS is potentially life threatening due to lung involvement, especially in rapidly progressive forms. Anti-histidyl-tRNA synthetase (anti-Jo1) antibodies are the most frequently detected antibodies in ASS (60 % of patients). Anti-threonyl-tRNA synthetase (anti-PL7) and alanyl-tRNA synthetase (anti-PL12) antibodies are each detected in 10 % of patients approximatively. Anti-tRNA-synthetases antibodies are mutually exclusive. Clinical heterogeneity of ASS patients appears to be associated with specific autoantibodies profile. Patients with anti-Jo1 antibodies have a more systemic presentation (especially with muscle involvement), whereas patients with anti-PL7 or anti-PL12 antibodies have more frequent and isolated ILD. If anti-PL7 and anti-PL12 antibodies are associated with more severe ILD and poorer survival is still matter of debate. Aims of this study were to compare ILD severity at diagnosis and clinical course in patients with ASS according to antisynthetase autoantibodies types.

NCT ID: NCT04923347 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

A Study to Evaluate the Safety and Efficacy of Fluticasone Furoate (FF)/Umeclidinium(UMEC)/Vilanterol (VI) in Participants With Chronic Obstructive Pulmonary Disease (COPD)

Start date: June 6, 2023
Phase: Phase 4
Study type: Interventional

This study will evaluate safety and efficacy of FF/UMEC/VI via ELLIPTA® inhaler. ELLIPTA is a registered trademark of GlaxoSmithKline group of companies.

NCT ID: NCT04922879 Completed - Pulmonary Disease Clinical Trials

Early Lung Rehabilitation Care for Patients After Double Lung Transplantation

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

Develop appropriate individual programs for patients to implement lung rehabilitation safely and effectively.

NCT ID: NCT04922554 Active, not recruiting - Clinical trials for Mycobacterium Infections, Nontuberculous

Oral Omadacycline vs. Placebo in Adults With NTM Pulmonary Disease Caused by Mycobacterium Abscessus Complex (MABc)

Start date: October 15, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy, safety and tolerability of oral omadacycline as compared to placebo in the treatment of adults with Nontuberculous Mycobacterial (NTM) pulmonary disease caused by Mycobacterium abscessus complex (MABc)

NCT ID: NCT04921943 Recruiting - Clinical trials for Nontuberculous Mycobacterium Infection

Hypertonic Saline for MAC

Start date: May 18, 2021
Phase: Phase 4
Study type: Interventional

The MAC-HS study is a testing whether hypertonic saline helps improve symptoms and clearance of mycobacteria in patients with M. avium complex lung infections.

NCT ID: NCT04921332 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Bright Light Therapy for Depression Symptoms in Adults With Cystic Fibrosis (CF) and COPD

Start date: September 7, 2021
Phase: N/A
Study type: Interventional

This is a project that will determine whether the use of daily bright light therapy has an effect on depressive symptoms experienced by adult inpatients with CF and COPD. The purpose of this project is to apply a daily 30-minute BLT intervention to hospitalized adult CF and COPD patients in order to decrease symptoms of depression as measured by depression inventory scoring.

NCT ID: NCT04919200 Completed - Clinical trials for Obstructive Lung Disease

Optimized Single-breath Helium Lung Volume in Obstructive Lung Disease

Start date: January 1, 2018
Phase:
Study type: Observational

Whole-body plethysmography (WBP) is the gold standard for measuring lung volume, but its clinical application is limited because it requires expensive equipment and is complicated to use. Studies have shown that the single-breath helium dilution (SBHD) method, which is commonly used in clinical practice, significantly underestimates lung volume in patients with obstructive lung disease (OLD). Therefore, by comparing the differences in lung volume measured by the SBHD method and WBP in patients with different severities of obstructive lung disease, we aim to establish a correction equation for the SBHD method to determine the total lung volume in obstructive lung disease patients.

NCT ID: NCT04918095 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

CareCOPD - COPD Home Monitoring Study

Start date: November 9, 2020
Phase:
Study type: Observational

This is a pilot study to demonstrate early validation of objective home-monitoring of Chronic obstructive pulmonary disease (COPD) patients by combining accurate and relevant patient data of medication and lung function (lung impedance) through patient-facing devices.

NCT ID: NCT04913961 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Supine Daoyin in the Treatment of AECOPD

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this study was to evaluate the clinical efficacy and safety of supine daoyin in the treatment of AECOPD.