Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to COPD from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 21
- Active, not recruiting: 8
- Completed: 11
- Other: 10
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT05061368 — Oral Sildenafil for Exercise Capacity, Dyspnea and Cardiopulmonary Function in COPD
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | University of Alberta |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
| Interventions | ; |
Chronic obstructive pulmonary disease (COPD) is a condition characterized by airway obstruction. Patients with COPD experience significant shortness of breath on exertion. The mechanisms responsible for shortness of breath on exertion are well understood in moderate and severe COPD, but, are poorly understood in mild COPD where symptoms appear disproportionate to the degree of airway obstructio…
NCT05163600 — The Acute Cardiorespiratory Response to Blood-flow Restricted Versus Traditional Exercise Training Regimens (CaRe BFR)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Zurich |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD |
| Interventions | ; ; |
The investigators hypothesize that BFR exercise regimens result in a different acute cardiorespiratory response pattern compared to traditional exercise regimens. Furthermore, the investigators hypothesize that these patterns differ between healthy participants and participants with COPD.
Regarding secondary objective, the investigators hypothesize that BFR results in lower blood pressure resp…
NCT05708443 — Effect of Combined Endurance Training on ADL and Walking in COPD Patients
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Istituti Clinici Scientifici Maugeri SpA |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD |
| Interventions | ; |
Chronic Obstructive Pulmonary Disease (COPD) is a chronic disease with related exercise intolerance and marked disability due to symptoms such as dyspnea and fatigue. Effort intolerance and exercise-induced symptoms cause marked impairment in completing activities of daily living (ADL). Pulmonary rehabilitation (PR), which has exercise as a major component, is considered a key treatment in the …
NCT05878769 — A Study to Evaluate the Long-Term Safety of Astegolimab in Participants With Chronic Obstructive Pulmonary Disease (COPD)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Hoffmann-La Roche |
| Enrollment | 2000 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
| Interventions |
The purpose of this study is to assess the long-term safety and to explore the efficacy of astegolimab in participants with chronic obstructive pulmonary disease (COPD) who have completed the 52-week placebo-controlled treatment period in parent studies GB43311 or GB44332.
NCT06283966 — A Study Evaluating the Efficacy of Budesonide, Glycopyrronium and Formoterol Fumarate Metered Dosed Inhaler on Cardiopulmonary Outcomes in Chronic Obstructive Pulmonary Disease
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | AstraZeneca |
| Enrollment | 5250 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD (Chronic Obstructive Pulmonary Disease) |
| Interventions | ; |
This study will evaluate the effect of triple ICS/LAMA/LABA therapy with BGF MDI 320/14.4/9.6 μg on cardiopulmonary outcomes relative to LAMA/LABA therapy with GFF MDI 14.4/9.6 μg in a population with COPD and elevated cardiopulmonary risk.
NCT06497816 — Health Literacy, Physical and Cognitive Function, Health-related Behaviors, and Quality of Life in COPD
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Hacettepe University |
| Enrollment | 144 |
| Study Type | OBSERVATIONAL |
| Conditions | COPD; Health Literacy; Health-Related Behavior |
| Interventions |
Health literacy is important for controlling disease progression and living a healthy life with illness. High health literacy is associated with higher cognitive performance and lower health-related quality of life. Physical, psychological, and social impairments are seen in chronic obstructive pulmonary disease (COPD). Studies investigating the relationship between health literacy and function…
NCT06603246 — A Study to Test the Safety and Effects of Inhaled GDC-6988 in Participants With Muco-obstructive Disease
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Genentech, Inc. |
| Enrollment | 128 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-cystic Fibrosis Bronchiectasis; Chronic Obstructive Pulmonary Disease |
| Interventions |
This study evaluates the safety, tolerability, and activity of inhaled GDC-6988 in participants with muco-obstructive disease.
NCT06883305 — A Study to Investigate the Efficacy and Safety of Tezepelumab in Adult Participants With Moderate to Very Severe COPD (D5241C00006)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | AstraZeneca |
| Enrollment | 990 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD) |
| Interventions | ; |
A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Tezepelumab in Adults with Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD)
NCT06944925 — A Study of BBT002 in Healthy Volunteers (HVs) and in Adult Patients With Chronic Obstructive Pulmonary Disease (COPD) or Chronic Rhiosininusitis With Nasal Polyps (CRSwNP)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Bambusa Therapeutics |
| Enrollment | 286 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
| Interventions | ; |
Randomized study of single and multiple doses of BBT002 in healthy volunteers and in adult patients with chronic obstructive pulmonary disease (COPD) or chronic rhinosinusitis with nasal polyps (CRSwNP).
NCT06985225 — Evaluation of Ventilation Defects Downstream of Mucus Plugs in Patients With Muco-Obstructive Lung Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Kansas Medical Center |
| Enrollment | 8 |
| Study Type | OBSERVATIONAL |
| Conditions | Severe Asthma; COPD; Non-CF Bronchiectasis; Cystic Fibrosis (CF) |
| Interventions |
In this study, xenon MRI will be used to evaluate regional functional consequences of mucus plugs in the lungs of patients with muco-obstructive pulmonary disease. Mucus plugs will be identified using CT imaging, and xenon MRI will be used to evaluate ventilation and gas exchange impairments in regions of the lungs corresponding to the airways downstream of mucus plugs.
NCT07030881 — Effect of Spacer Use on Exacerbation Risk in High-Risk Older Adults With Chronic Airway Diseases Receiving Triple Therapy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | First Affiliated Hospital of Ningbo University |
| Enrollment | 380 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma, COPD |
| Interventions | ; |
This study evaluates whether adding a spacer device to triple inhaled therapy (ICS/LABA/LAMA via pMDI) can reduce acute exacerbations in elderly patients (≥65 years) with stable chronic airway diseases (COPD or asthma) who are classified as high-risk based on GOLD or GINA guidelines. High risk is defined as ≥1 hospitalization or ≥2 moderate exacerbations in the past 12 months.
Despite receivin…
NCT07097896 — Endobronchial Silicone Valve for Patients With Emphysema
| Status | Recruiting |
| Phase | N/A |
| Sponsor | China-Japan Friendship Hospital |
| Enrollment | 147 |
| Study Type | INTERVENTIONAL |
| Conditions | Emphysema |
| Interventions | ; |
The purpose of this research is to evaluate the efficacy and safety of endobronchial silicone valve in patients with severe emphysema.
NCT07073950 — A Study to Investigate the Effect of Budesonide/Glycopyrronium/Formoterol Fumarate Metered Dose Inhaler (BGF MDI) Compared With Placebo MDI on Heart and Lung Function in Participants With Chronic Obstructive Pulmonary Disease (COPD) and Hyperinflation
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | AstraZeneca |
| Enrollment | 56 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease; Hyperinflation |
| Interventions | ; ; |
The purpose of the study is to evaluate the effect of BGF MDI compared with placebo MDI on cardiac and lung function when administered in participants diagnosed with COPD and hyperinflation.
NCT06909773 — The Prevalence of COPD in Patients With Cardiovascular Disease and the Benefit of Cardiopulmonary Co-management
| Status | Recruiting |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 3000 |
| Study Type | INTERVENTIONAL |
| Conditions | Cardiovascular Diseases |
| Interventions |
This is a multi-center, prospective, and interventional study conducted in 3 types of cardiovascular diseases (CVD) participants , including 3 cohorts which are patients with newly or previously diagnosed coronary heart disease ( CHD), atrial fibrillation ( AF) and chronic heart failure (CHF).
NCT07069829 — Study of Clinical and Patient-reported Outcomes in Adults With Moderate to Severe COPD Treated With Breztri/Trixeo
| Status | Recruiting |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 1400 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
Chronic Obstructive Pulmonary Disease is a leading cause of global morbidity and mortality, especially in low- and middle-income countries. Exacerbations accelerate disease progression and increase the risk of death. Recent recommendations from the GOLD report emphasize the diagnosis of COPD and treatment planning based on a combination of lung function metrics, exacerbation history, and patien…
NCT07602192 — Quantitative Chest CT and Multi-Omics to Distinguish Asthma From COPD and Predict Treatment Response
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Korea University Guro Hospital |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Asthma (Diagnosis); COPD (Chronic Obstructive Pulmonary Disease) |
This study aims to improve the diagnosis and treatment prediction of asthma and chronic obstructive pulmonary disease (COPD) by combining quantitative chest computed tomography (CT) imaging with multi-omics data.
Adults with asthma or COPD will be enrolled and undergo routine clinical evaluations, pulmonary function tests, blood tests, and chest CT scans. Additional samples, such as sputum and…
NCT07566195 — Long-term Safety and Tolerability of Tozorakimab in Patients With COPD and History of Exacerbations
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | AstraZeneca |
| Enrollment | 61 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease; COPD |
| Interventions | ; |
ROMEO is a Phase III, multicentre, open-label, chronic-dosing extension study evaluating the long-term safety of two dose regimens of tozorakimab in participants with COPD and a history of exacerbations.
Eligible participants must have completed one of the predecessor studies.
NCT07665931 — Effect of Simeox® on Residual Volume in COPD Patients With Pulmonary Hyperinflation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Azienda Socio Sanitaria Territoriale di Lodi |
| Enrollment | 23 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD); Pulmonary Hyperinflation |
| Interventions |
Brief Summary People with severe chronic obstructive pulmonary disease (COPD) often have too much air trapped in their lungs (pulmonary hyperinflation). This makes it hard to breathe and reduces quality of life. This study tests whether a single session with a medical device called Simeox® can reduce the amount of air trapped in the lungs. Simeox® works by applying gentle intermittent negative …
NCT07474220 — Expression of SLC25A48 in Chronic Obstructive Pulmonary Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fu Jen Catholic University |
| Enrollment | 180 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
This study aims to investigate the expression level of SLC25A48, a mitochondrial choline transporter, in peripheral blood mononuclear cells of patients with chronic obstructive pulmonary disease, and to analyze its correlation with inflammatory markers and choline metabolic byproducts.
NCT07447232 — Comparing Ultrasonic and Conventional Spirometry in Chronic Respiratory Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fu Jen Catholic University |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD); Spirometry |
| Interventions |
This study compares a handheld ultrasonic spirometer with a standard hospital spirometer in adults with chronic respiratory diseases. Each participant will complete lung function tests using both devices. The study aims to determine whether the ultrasonic device provides accurate and reliable measurements for use in clinical or home settings.
NCT07684820 — To Evaluate the Effect of EXPD-101/FXS7553 Compared With Placebo in Patients With COPD Over 52 Weeks of Treatment
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Expedition Therapeutics, Inc |
| Enrollment | 600 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD) |
| Interventions | ; ; |
This is a Phase 2 study of the efficacy, safety, tolerability and pharmacokinetics of two doses of EXPD-101 in participants with COPD. Study participants will be randomized to receive either study drug or placebo administered once daily for 52 weeks.
Active, Not Recruiting
NCT03256773 — High Resolution Micro OCT Imaging
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 160 |
| Study Type | OBSERVATIONAL |
| Conditions | Cystic Fibrosis; COPD; PCD - Primary Ciliary Dyskinesia; Covid19; Sinusitis |
The purpose of this study is to learn about using the imaging to make images of the lungs and nose with the long-term goal of the research leading to potential treatments and new therapies for patients with cystic fibrosis.
NCT04212962 — Transitional Care Model Evaluation 2020
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Mathematica Policy Research, Inc. |
| Enrollment | 962 |
| Study Type | INTERVENTIONAL |
| Conditions | CHF - Congestive Heart Failure; COPD; Pneumonia |
| Interventions | ; |
The study is a randomized controlled trial to estimate the effects of the transitional care model (TCM) on hospital admissions and patients’ experience during the year following the patient’s qualifying discharge. The University of Pennsylvania, where TCM was developed, will be the coordinating center for the implementation. The study will be conducted in three large health systems spread throu…
NCT04536675 — Effect of Perioperative Bronchodilator in COPD Patients Undergoing Lung Cancer Surgery
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Samsung Medical Center |
| Enrollment | 204 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease; Non Small Cell Lung Cancer |
| Interventions | ; |
This is a double-blind randomized controlled trial evaluating the effect of perioperative dual bronchodilator therapy on post-operative pulmonary function and health-related quality of life (QoL) in mild-to-moderate less symptomatic COPD patients undergoing lung cancer surgery.
Investigators hypothesized that dual bronchodilator, as compared with placebo, would prevent reduction of pulmonary f…
NCT04968249 — Michigan Early Disease Progression Cohort
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Michigan |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | COPD |
| Interventions |
The aim of this project is to develop a disease progression cohort within the University of Michigan Health System to capture pulmonary function, symptom assessments and quantitative imaging among patients at risk for or with an established diagnosis of COPD, focusing however on “early” COPD (age 30-55 and GOLD stage 0,1, 2, and prism).
NCT06601777 — Evaluation of the Effectiveness, Safety, and Cost of a Smart Hospital System for Patients With Chronic Obstructive Pulmonary Disease
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Yonsei University |
| Enrollment | 196 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
| Interventions | ; |
This study aims to analyze the effectiveness/safety/cost of the Smart Homespital system that provides a service that allows patients with Chronic Obstructive Pulmonary Disease to easily access and use biosignals generated using biosignal collection medical equipment at home.
NCT06969573 — Inhaled Treprostinil for Dyspnea and Exercise Intolerance in Mild COPD
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | University of Alberta |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD (Chronic Obstructive Pulmonary Disease) |
| Interventions | ; ; |
The goal of this clinical trial is to evaluate the impact of inhaled Treprostinil on breathlessness and low exercise capacity in patients living with mild chronic obstructive pulmonary disease. Participants will be asked to:
- Perform lung function and exercise tests
- Have ultrasound of their heart
- Have CT images of their lungs
- Visit the lab on 5 different occasions (plus one visit to the…
NCT07687836 — Retrospective Evaluation of the Implementation of a Digital Solution Supporting the Delivery of Pulmonary Rehabilitation Programs in Private Physiotherapy Practice
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | ADIR Association |
| Enrollment | 50 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD); Respiration Disorders; Pulmonary Rehabilitation; Chronic Respiratory Diseases |
| Interventions |
Pulmonary rehabilitation improves exercise capacity, functional status, symptoms and quality of life in individuals with chronic respiratory diseases. However, access to pulmonary rehabilitation remains limited due to insufficient availability of specialized centers and geographical, organizational, logistical, and financial barriers. Delivering pulmonary rehabilitation in private physiotherapy…
NCT07118189 — Laying the Foundation for Building a Resilient KPNC Community in the Face of Worsening Air Quality Due to Wildfire Smoke
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Kaiser Permanente |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD); Exacerbation of COPD; Exacerbation of Chronic Obstructive Pulmonary Disease |
| Interventions |
The overarching goal of this project is to conduct a pilot intervention in high-risk Kaiser Permanente Northern California patients with chronic obstructive pulmonary disease to mitigate their exposure to poor air quality and decrease exacerbations of lung disease.
Not Yet Recruiting
NCT07679646 — Effectiveness and Efficiency of Home Telemonitoring and Non-invasive Ventilation in Patients With COPD and Hypercapnia (EVALECO)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Air Liquide Healthcare Spain |
| Enrollment | 92 |
| Study Type | OBSERVATIONAL |
| Conditions | Pulmonary Disease, Chronic Obstructive (COPD); Hypercapnia |
| Interventions |
The purpose of this study is to evaluate the effectiveness and clinical efficiency of combining home non-invasive ventilation (NIV) with a continuous remote telemonitoring (TM) system in patients with Chronic Obstructive Pulmonary Disease (COPD) and persistent hypercapnia. In standard practice, patients with severe COPD and high carbon dioxide levels in their blood are treated with home non-inv…
NCT07684391 — Effect of Oral Astaxanthin Formula on Pulmonary Rehabilitation in Patients With COPD
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | China-Japan Friendship Hospital |
| Enrollment | 140 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD |
| Interventions | ; |
The goal of this clinical trial is to investigate whether an astaxanthin-based dietary supplement combined with a pulmonary rehabilitation training program could improve exercise capacity in patients with COPD. The main questions it aims to answer are:
• whether an astaxanthin-based dietary supplement combined with a pulmonary rehabilitation training program could improve 6MWD in patients with…
NCT07668518 — A Study of the Safety, Tolerability, Pharmacokinetics and Efficacy of KIT2014 in Patients With Moderate to Severe COPD
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Kither Biotech Srl |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD) |
| Interventions | ; |
Study investigating the safety, tolerability, pharmacokinetics and early efficacy with KIT2014 over 7 days of treatment in moderate to severe chronic obstructive pulmonary disease patients.
NCT07666854 — Tele-Pulmonary Rehabilitation For COPD Patients Living in Peripheral Areas
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Tel-Aviv Sourasky Medical Center |
| Enrollment | 110 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD (Chronic Obstructive Pulmonary Disease); Rehabilitation; Peripheral |
| Interventions |
Pulmonary rehabilitation (PR) is a key non-pharmacological intervention for patients with chronic obstructive pulmonary disease (COPD), yet it remains underutilized, particularly among patients living in peripheral areas due to limited access, travel distance, and logistical barriers. Tele-pulmonary rehabilitation (TPR) has the potential to improve access to care, but its feasibility and effect…
NCT07612878 — The Study of Chronic Obstructive Pulmonary Disease (COPD) Participants Treated With Dupilumab (STRIDE) Registry
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Sanofi |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | COPD (Chronic Obstructive Pulmonary Disease) |
| Interventions | ; |
The STRIDE Registry will evaluate the real-world effectiveness and safety of dupilumab in participants with COPD. The primary objective is to describe characteristics of participants newly initiated with dupilumab for COPD. Secondary objectives are to determine whether treatment with dupilumab reduces moderate and/or severe COPD exacerbations; to determine the impact of treatment on lung functi…
NCT07682168 — DIVision of the Interlobar Fissure in Patients Who Do Not Respond to Endobronchial Lung Volume Reduction
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Rocco Bilancia |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD); Emphysema; Lung Volume Reduction Surgery |
| Interventions |
Surgical division of fissure is hypothesized to be safe and feasible. However, there is no preparatory study to test this hypothesis. It is logically expected that morbidity from the procedure could be less than standard LVRS and in preparation to a side-to-side trial of fissure division versus standard LVRS, a safety and feasibility study is required to test this hypothesis and inform future t…
NCT07686302 — Feasibility of Noninvasive Trigeminal Nerve Stimulation During Exercise
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Johns Hopkins University |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD |
| Interventions | ; ; |
The purpose of this study is to examine 1) effects of cutaneous electrical trigeminal nerve stimulation (eTNS) on respiratory control in healthy volunteers and 2) explore the potential of this approach to mitigate dyspnea in patients with chronic obstructive lung disease (COPD).
NCT07668921 — Acute Muscular and Vascular Responses to a Single Session of Exercise With BFR in COPD
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Grenoble |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Control Condition; Pulmonary Disease (COPD), Chronic Obstructive; Blood Flow Restriction Training (BFRT) |
| Interventions | ; |
Exercise training is a cornerstone of pulmonary rehabilitation (PR) in patients with chronic obstructive pulmonary disease (COPD). However, some patients derive limited benefits from conventional exercise programs. Previous studies suggest that the magnitude of exercise-induced muscle fatigue is associated with training effectiveness, with patients unable to develop significant muscle fatigue (…
NCT04820257 — Home-based Pulmonary Rehabilitation for COPD Patients
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Karolinska Institutet |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD, Chronic Obstructive Pulmonary Disease |
| Interventions |
Objectives The objective of this project is to motivate patients with COPD to incorporate the habit of doing daily mindful physical activity by using the proposed home-based pulmonary rehabilitation program that integrates video guided exercises, activity monitoring daily steps and health coaching. This program will allow patients to complete Pulmonary Rehabilitation (PR) at home and promote be…
NCT04231760 — The Effect of Inhaled Nitric Oxide on Pulmonary Gas-exchange in COPD
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | University of Alberta |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
| Interventions | ; |
Chronic Obstructive Pulmonary Disease (COPD) is a lung disorder commonly caused by smoking, which makes breathing more difficult. When COPD patients exercise, they are not efficient breathers and this leads to serious breathing difficulties, which often causes these patients to stop exercise at low intensities. Even though patients with a mild form of COPD have relatively well preserved lung fu…
Completed Trials
NCT03152669 — The Extended Salford Lung Study (“Ex-SLS”) Data Access Project
| Status | Completed |
| Phase | N/A |
| Sponsor | GlaxoSmithKline |
| Enrollment | 1183 |
| Study Type | OBSERVATIONAL |
| Conditions | Asthma |
The Salford Lung Study (SLS) subjects represent a group of COPD and asthma patients whose disease is extremely well-characterised over a short time period. Subjects in the SLS originally consented for information relevant to the study to be shared with the sponsor (GSK). These data were limited to three years prior to randomisation and the twelve-month interventional treatment period. Broadened…
NCT04069312 — Roflumilast or Azithromycin to Prevent COPD Exacerbations Trial
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Johns Hopkins University |
| Enrollment | 1032 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease Severe; Chronic Bronchitis |
| Interventions | ; |
A multi-center, randomized, 72-month, parallel- group, non-inferiority, phase III study to compare the effectiveness of roflumilast (Daliresp, 500 mcg quaque die (QD) or alternate regimen) therapy versus azithromycin (250 mg QD, 500 mg QD three times per week, or alternate regimen) to prevent hospitalization or death in a patients at high risk for COPD exacerbations.
NCT05568043 — The Reducing REVISITS Study: A Cluster RCT
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Chicago |
| Enrollment | 384 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD; COPD Exacerbation Acute |
| Interventions | ; |
This type II hybrid effectiveness-implementation trial will concurrently study the comparative effectiveness of virtual vs. in-person COPD care transition programs implemented via virtual mentored implementation approaches with and without co-design methods.
The investigators will enroll up to 24 randomized sites (with a goal minimum of 16 sites) to:
- Deliver the COPD programs implemented vi…
NCT05352490 — Diagnosis of Heart Failure in Chronic Obstructive Pulmonary Disease Using the Lung Ultrasound
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Monastir |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | Dyspnea; Decompensated Heart Failure ; COPD Exacerbation |
| Interventions |
Acute Heart failure (AHF) is a common cause of acute exacerbation of chronic obstructive pulmonary disease (AECOPD). This association is frequently underestimated with regard to the difficulty of clinical diagnosis. The investigators expect that the application of the lung ultrasound could be useful in this issue.
NCT05572333 — Clinical Trial to Investigate the Safety and Tolerability of EP395 in Patients With COPD
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | EpiEndo Pharmaceuticals |
| Enrollment | 61 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease; COPD |
| Interventions | ; |
The aim of this clinical trial is to investigate the safety and tolerability of oral, once-daily EP395 administration in COPD patients for 12 weeks.
NCT04119934 — Personalized Smoking Cessation Infographic in COPD
| Status | Completed |
| Phase | N/A |
| Sponsor | Unity Health Toronto |
| Enrollment | 83 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD); Smoking Cessation |
| Interventions |
This study assesses the effect of a personalized smoking cessation infographic on physician smoking cessation counseling rates and smoking cessation pharmacotherapy prescription rates. The study assesses the difference in physician behaviour using an interrupted time series analysis (one-year pre vs. one-year post-intervention). General practitioners, nurse practitioners and respirologists who …
NCT05742802 — Long-term Efficacy and Safety of Tozorakimab in Participants With Chronic Obstructive Pulmonary Disease With a History of Exacerbations (PROSPERO).
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | AstraZeneca |
| Enrollment | 1713 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD) |
| Interventions | ; ; |
Subjects who completed either OBERON or TITANIA will be offered the opportunity to consent for this Multicentre, Double-blind, Randomised, Placebo controlled, Parallel Group, Phase 3, extension study to evaluate the safety and efficacy of Tozorakimab in adult participants with symptomatic COPD.
NCT06336252 — Technology Assisted Nudging to Increase Physical Activity Among Hospitalised Medical Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | Bispebjerg Hospital |
| Enrollment | 130 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD; Heart Failure; Parkinson Disease; Arthritis; Old Age; Cachexia |
| Interventions |
Primary Objective To investigate if patients hospitalised for older adults with a decreased level of physical function, either related to a chronic condition e.g., COPD, Congestive heart failure, renal failure; infections; frailty and tendency of falling; orthopaedic surgery - after hip fracture will increase their time spent out of bed during hospitalisation and 3 months after discharge throug…
NCT06511193 — Chronicling the COPD Patient Journey and Change in COPD Symptoms, Quality of Life and Exacerbations Following Initiation of Budenoside/Glycopyrronium/Formoterol [BGF]
| Status | Completed |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 152 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD) |
| Interventions |
The CHRONICLES study will investigate the change in clinical and patient reported outcomes after six-months of treatment with Budenoside/Glycopyrronium/Formoterol [BGF] in a real-world setting.
NCT06863246 — Postural Control in Chronic Obstructive Pulmonary Disease
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer |
| Enrollment | 36 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD) |
| Interventions | ; |
Postural control impairment is common in people with COPD (pwCOPD), which can increase the risk of falls and affect quality of life. However, the majority of existing studies examine this postural control in isolation, without taking into account the cognitive demands that occur during activities of daily living during which individuals are often required to perform a mental task while maintain…
NCT06871670 — Force Control in Chronic Obstructive Pulmonary Disease
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer |
| Enrollment | 36 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD) |
| Interventions |
Maximal muscle strength is one of the most commonly assessed neuromuscular parameters in people with COPD due to its accessibility and relevance for prescribing an appropriate workload for resistance training. However, maximal force production is very rarely necessary during daily activities which requires production of submaximal and precisely controlled forces. Despite growing research on mot…