Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06072690
Other study ID # COPDCVS1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 15, 2021
Est. completion date August 31, 2026

Study information

Verified date October 2023
Source Lithuanian University of Health Sciences
Contact Skaidrius Miliauskas, PhD, Prof.
Phone +37037326269
Email skaidrius.miliauskas@lsmu.lt
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Chronic obstructive pulmonary disease (COPD) is a major cause of disability and death worldwide. People with COPD often have cardiovascular diseases (CVDs) that are associated with increased risk for hospitalization and prolonged stay as well as all-cause and CVD-related mortality. Nevertheless, CVDs in patients with COPD are tend to be underestimated in clinical practice. Mechanisms that define the relation between COPD and cardiovascular morbidity include lung hyperinflation, hypoxia, pulmonary hypertension, systemic inflammation and oxidative stress, exacerbation, shared risk factors and COPD phenotypes. Recently, some authors have announced that COPD treatment with dual bronchodilation may not only improve pulmonary function and quality of life, but also have a positive effect on cardiac function in cardiac magnetic resonance imaging (MRI) or two-dimensional cardiac ultrasound for the assessments. The aim of this study is to specify the state of respiratory and cardiovascular systems as well as exercise capacity and quality of life in patients with newly diagnosed moderate-to-severe COPD and to evaluate their changes after short-term treatment with dual bronchodilation. We hypothesize that patients with newly diagnosed COPD and no previous records of cardiac diseases and no apparent signs of heart failure have significantly impaired cardiac autonomic integrity that precedes to increased risk of cardiovascular events. It is believed that cardiac autonomic integrity might significantly improve with dual bronchodilation therapy.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date August 31, 2026
Est. primary completion date August 31, 2026
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: - Aged 40 years and older - Smoking index of 10 pack-years and more - Newly diagnosed chronic obstructive pulmonary disease (COPD) with forced expiratory volume in 1 second (FEV1) 30-79 percent of predicted and forced expiratory volume in 1 second to forced vital capacity ratio (FEV1/FVC) less than 70 percent of predicted. Exclusion Criteria: - Active lung infection - Present or previously treated lung cancer - Alpha-1 antitrypsin deficiency - Diagnosed interstitial lung disease - Previously diagnosed asthma - Diagnosed chronic hypercapnic respiratory failure - Treatment with systemic glucocorticoids - Unstable ischaemic heart disease - Pregnancy - Present cardiac arrhythmias - Uncontrolled arterial hypertension - Dementia and other mental states that determine patient's inability to consent - Other medical conditions that in the opinion of the investigator disqualify the subject for inclusion

Study Design


Locations

Country Name City State
Lithuania Lithuanian University of Health Sciences Kaunas

Sponsors (1)

Lead Sponsor Collaborator
Lithuanian University of Health Sciences

Country where clinical trial is conducted

Lithuania, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in exercise capacity at week 12 The effect of dual bronchodilation on exercise capacity (6 minute walk distance test and cardiopulmonary exercise test results) in patients with newly diagnosed moderate-to-severe chronic obstructive pulmonary disease Baseline and week 12
Primary Change from baseline in Short Form 36 Health Survey Questionnaire at week 12 The effect of dual bronchodilation on quality of life (Short Form 36 Health Survey Questionnaire (SF-36) results) in patients with newly diagnosed moderate-to-severe chronic obstructive pulmonary disease Baseline and week 12
Secondary Change from baseline in forced expiratory volume in 1 second at week 12 The effect of dual bronchodilation on forced expiratory volume in 1 second (FEV1) in patients with newly diagnosed moderate-to-severe chronic obstructive pulmonary disease Baseline and week 12
Secondary Change from baseline in forced vital capacity at week 12 The effect of dual bronchodilation on forced vital capacity (FVC) in patients with newly diagnosed moderate-to-severe chronic obstructive pulmonary disease Baseline and week 12
Secondary Change from baseline in diffusing capacity of the lungs for carbon monoxide at week 12 The effect of dual bronchodilation on diffusing capacity of the lungs for carbon monoxide (DLCO) in patients with newly diagnosed moderate-to-severe chronic obstructive pulmonary disease Baseline and week 12
Secondary Change from baseline in airway resistance at week 12 The effect of dual bronchodilation on airway resistance (described as specific air resistance (sRaw) and total airway resistance (Raw tot)) in patients with newly diagnosed moderate-to-severe chronic obstructive pulmonary disease Baseline and week 12
Secondary Change from baseline in residual volume at week 12 The effect of dual bronchodilation on residual volume (RV) in patients with newly diagnosed moderate-to-severe chronic obstructive pulmonary disease Baseline and week 12
Secondary Change from baseline in residual volume to total lung capacity ratio at week 12 The effect of dual bronchodilation on residual volume to total lung capacity ratio (RV/TLC) in patients with newly diagnosed moderate-to-severe chronic obstructive pulmonary disease Baseline and week 12
Secondary Change from baseline in forced residual capacity to total lung capacity ratio at week 12 The effect of dual bronchodilation on forced residual capacity to total lung capacity ratio (FRC/TLC) in patients with newly diagnosed moderate-to-severe chronic obstructive pulmonary disease Baseline and week 12
Secondary Change from baseline in right ventricle end-systolic volume index at week 12 The effect of dual bronchodilation on right ventricle end-systolic volume index (RVESVi) in patients with newly diagnosed moderate-to-severe COPD Baseline and week 12
Secondary Change from baseline in right ventricle end-diastolic volume index at week 12 The effect of dual bronchodilation on right ventricle end-diastolic volume index (RVEDVi) in patients with newly diagnosed moderate-to-severe COPD Baseline and week 12
Secondary Change from baseline in on left ventricle end-systolic volume index at week 12 The effect of dual bronchodilation on left ventricle end-systolic volume index (LVESVi) in patients with newly diagnosed moderate-to-severe COPD Baseline and week 12
Secondary Change from baseline in left ventricle end-diastolic volume index at week 12 The effect of dual bronchodilation on left ventricle end-diastolic volume index (LVEDVi) in patients with newly diagnosed moderate-to-severe COPD Baseline and week 12
Secondary Change from baseline in stroke volume index at week 12 The effect of dual bronchodilation on stroke volume index (SVi) in patients with newly diagnosed moderate-to-severe COPD Baseline and week 12
Secondary Change from baseline in right ventricular strains at week 12 The effect of dual bronchodilation on right ventricular strains in patients with newly diagnosed moderate-to-severe COPD Baseline and week 12
Secondary Change from baseline in washout rate at week 12 The effect of dual bronchodilation on washout rate (WR) in cardiac sympathetic imaging with meta-iodobenzylguanidine in patients with newly diagnosed moderate-to-severe COPD Baseline and week 12
Secondary Change from baseline in heart to mediastinum ratio at week 12 The effect of dual bronchodilation on early and late heart to mediastinum ratio (HMR) in cardiac sympathetic imaging with meta-iodobenzylguanidine in patients with newly diagnosed moderate-to-severe COPD Baseline and week 12
Secondary Change from baseline in left ventricle total defect score at week 12 The effect of dual bronchodilation on early and late left ventricle early total defect score (TDS) in cardiac sympathetic imaging with meta-iodobenzylguanidine in patients with newly diagnosed moderate-to-severe COPD Baseline and week 12
See also
  Status Clinical Trial Phase
Recruiting NCT05654272 - Development of CIRC Technologies
Recruiting NCT05650307 - CV Imaging of Metabolic Interventions
Recruiting NCT04515303 - Digital Intervention Participation in DASH
Completed NCT04056208 - Pistachios Blood Sugar Control, Heart and Gut Health Phase 2
Recruiting NCT04417387 - The Genetics and Vascular Health Check Study (GENVASC) Aims to Help Determine Whether Gathering Genetic Information Can Improve the Prediction of Risk of Coronary Artery Disease (CAD)
Not yet recruiting NCT06211361 - Cardiac Rehabilitation Program in Patients With Cardiovascular Disease N/A
Not yet recruiting NCT06032572 - Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE) N/A
Recruiting NCT04514445 - The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches.
Enrolling by invitation NCT04253054 - Chinese Multi-provincial Cohort Study-Beijing Project
Completed NCT03273972 - INvestigating the Lowest Threshold of Vascular bENefits From LDL Lowering With a PCSK9 InhibiTor in healthY Volunteers N/A
Completed NCT03680638 - The Effect of Antioxidants on Skin Blood Flow During Local Heating Phase 1
Recruiting NCT04843891 - Evaluation of PET Probe [64]Cu-Macrin in Cardiovascular Disease, Cancer and Sarcoidosis. Phase 1
Completed NCT04083846 - Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of High-dose CKD-385 in Healthy Volunteers(Fed) Phase 1
Completed NCT04083872 - Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of Highdose CKD-385 in Healthy Volunteers(Fasting) Phase 1
Completed NCT03619148 - The Incidence of Respiratory Symptoms Associated With the Use of HFNO N/A
Completed NCT03693365 - Fluid Responsiveness Tested by the Effective Pulmonary Blood Flow During a Positive End-expiratory Trial
Completed NCT03466333 - Postnatal Enalapril to Improve Cardiovascular fUnction Following Preterm Pre-eclampsia Phase 2
Completed NCT04082585 - Total Health Improvement Program Research Project
Completed NCT05132998 - Impact of a Comprehensive Cardiac Rehabilitation Program Framework Among High Cardiovascular Risk Cancer Survivors N/A
Completed NCT05067114 - Solutions for Atrial Fibrillation Edvocacy (SAFE)