Clinical Trials Logo

Idiopathic Pulmonary Fibrosis clinical trials

View clinical trials related to Idiopathic Pulmonary Fibrosis.

Filter by:

NCT ID: NCT04720443 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

A Safety, Tolerability, and Pharmacokinetic Study of NIP292 in Healthy Normal Subjects

Start date: November 22, 2019
Phase: Phase 1
Study type: Interventional

This study is being conducted to evaluate the safety and tolerability of single ascending and multiple ascending oral doses of NIP292 tablets administered following an overnight fast in healthy adult subjects.

NCT ID: NCT04586946 Completed - Clinical trials for Obstructive Sleep Apnea

FIBRotic Interstitial Lung Disease and Nocturnal OXygen

FIBRINOX
Start date: December 17, 2018
Phase:
Study type: Observational

Home sleep studies - which allow the measurement of breathing while the person sleeps - will be performed on patients with fibrotic interstitial lung disease attending two of the UK's largest respiratory medicine services.The study will investigate at how symptoms, and breathing and exercise tests differ between these two groups after 12 months of study.

NCT ID: NCT04572971 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Reliability and Validity of iOS in IPF

Start date: November 6, 2020
Phase:
Study type: Observational

Idiopathic pulmonary fibrosis (IPF) is a condition where scar tissue (called fibrosis) builds up in the lungs. It usually gets worse over time. Fibrosis causes the lungs to become stiff, and reduces the amount of oxygen that the lungs can take up. People with IPF complain of worsening breathlessness, which limits their day to day activities. Lung function tests are breathing tests that measure how well the lungs are working, and are used by doctors to decide whether to start or stop medicines in people with IPF. However, people with IPF tell us that lung function tests require a lot of effort, can make them cough and feel very short of breath. About 1 in 5 people with IPF are unable to perform lung function results accurately. Impulse oscillometry (iOS) is a new type of breathing test. It uses sound waves to measure the stiffness of the lung. The test is very quick (30 seconds), does not require any effort from the patient, and only requires a patient to breathe in their usual way. iOS has been used successfully in children who are unable to perform normal lung function tests. The investigators will assess whether people with IPF can perform iOS tests accurately and to compare their experiences of having iOS tests with their experience of performing current lung function tests. The investigators will also compare whether there is a relationship between iOS tests and the information gathered from the tests currently used by doctors to measure the impact of IPF (lung function tests, exercise tests, lung scans and questionnaires that measure quality of life).

NCT ID: NCT04564664 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

High-flow Oxygen Therapy During Exercise in Idiopathic Pulmonary Fibrosis

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

Objectives: 1. To evaluate endurance time during cardiopulmonary exercise test (CPET) performance comparing standard oxygen therapy to high-flow nasal cannula (HFNC) oxygen therapy in subjects with idiopathic pulmonary fibrosis (IPF) with exertional desaturation. 2. To assess oxygenation level (peripheral and muscular) as well as dyspnea and fatigue during exercise in IPF subjects with exertional desaturation using oxygen supplementation with HFNC compared with standard oxygen supplementation. Method: multicenter crossover clinical trial. Patients with IPF presenting oxygen desaturation during the six-minute walking test (6MWT) (SpO2 mean ≤ 85%) will be included consecutively . Each subject evaluated will perform initially an incremental CPET to evaluate the patient's maximum exercise capacity. Supplemental oxygen will be applied to maintain SpO2 >85% with a Venturi mask. Maximum exercise capacity and the appropriate final oxygen inspiratory fraction (FiO2) needed for the following tests will be determined. Posteriorly each patient will perform two constant load CPET (at 75% of the maximum workload achieved with the incremental CPET); one with standard oxygen therapy and the other one with HFNC oxygen therapy. Endurance time, dyspnea and leg fatigue and oxygen saturation (peripheral and muscular) will be recorded. Evaluation measures: Endurance time, dyspnea and leg fatigue (Borg scale), and oxygen saturation.

NCT ID: NCT04533022 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Safety, Efficacy and Pharmacokinetics of C21 in Subjects With IPF

Start date: November 13, 2020
Phase: Phase 2
Study type: Interventional

This trial is a multi-centre, open-label, single-arm phase 2 trial investigating the safety, efficacy and pharmacokinetics of C21 in subjects with idiopathic pulmonary fibrosis.

NCT ID: NCT04525547 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Safety and Effectiveness of Nintedanib in Korean Patients

Start date: January 13, 2021
Phase:
Study type: Observational

The objectives of this study are to monitor the safety and effectiveness of Ofev in Korean patients in a routine clinical practice setting.

NCT ID: NCT04512170 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Single and Multiple Dose Safety, Tolerability, PK and Food Effect Study of HEC585 in Healthy Male and Female Subjects

Start date: July 13, 2020
Phase: Phase 1
Study type: Interventional

The Safety, Tolerability Pharmacokinetic and Food Effect Study of HEC585 in Healthy Male and Female Subjects

NCT ID: NCT04481074 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Inspiratory Muscle Training in Patients With Interstitial Lung Disease

IMT-ILD
Start date: July 30, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effects of inspiratory muscle training program in inspiratory muscle endurance, breathlessness, inspiratory muscle strength, functional capacity and quality of life in patients with interstitial lung disease. Patients are evaluated before the inspiratory muscle training and after 8 weeks of training.

NCT ID: NCT04430491 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

To Evaluate the Use of Radiomics to Classify Between Idiopathic Pulmonary Fibrosis and Interstitial Lung Disease

Start date: January 1, 2005
Phase:
Study type: Observational

To investigate the ability of machine learning models based on radiomic features extracted from thin-section CT images to differentiate IPF patients from non-IPF interstitial lung diseases.

NCT ID: NCT04429516 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Morphine Sulfate/Placebo for the Treatment of PulmonAry Fibrosis Cough

PAciFy Cough
Start date: December 17, 2020
Phase: Phase 3
Study type: Interventional

Idiopathic pulmonary fibrosis (IPF) is a disease of unknown cause that results in scarring of the lungs. Cough is reported by 85% of patients with IPF and can be a distressing symptom with significant physical, social and psychological consequences particularly anxiety and depression. The cause of cough in IPF is poorly understood and there are currently no proven effective therapies. Morphine has long been advocated for the suppression of chronic cough in other conditions. While morphine is frequently used as a palliative agent for breathlessness in IPF, its effects on cough have never been tested. The aim of this study is therefore to explore and compare the effect of low dose morphine, one of the few therapies shown to be effective in some patients with otherwise refractory chronic cough, in patients with IPF, to an inactive substance known as a placebo. To make a fair comparison, patients will be randomly allocated to receiving either morphine or placebo in a blinded fashion. This means neither the doctor nor the patient will know which drug they are receiving, and the drugs will appear the same. However, the trial is designed so that you will receive both morphine and placebo, but at different times (this is called a cross-over study). More specifically, you will be given either morphine or placebo for 14 days at a time. In this study, it is hypothesised that compared with placebo, low dose (5mg) controlled release Morphine sulfate (MST) will reduce the number of coughs recorded during a 24hr period in patients with IPF.