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Bronchiectasis clinical trials

View clinical trials related to Bronchiectasis.

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NCT ID: NCT04435327 Completed - COVID Clinical Trials

Lung Damage Caused by SARS-CoV-2 Pneumonia (COVID-19)

SequelaeCov
Start date: October 5, 2020
Phase:
Study type: Observational

Pneumonia is a recurrent element of COVID-19 infection, it is often associated with development of respiratory failure and patients frequently need various degrees of oxygen therapy up to non invasive ventilation (NIV-CPAP) and invasive mechanical ventilation (IMV). Main purpose of this study is to evaluate with non invasive clinical instruments (pletysmography, Diffusion lung capacity for carbon monoxide -DLCO-, six minute walking test and dyspnea scores) and radiological tools (chest X-ray and chest CT scan) the development of medium-to-long term pulmonary sequelae caused by SARS-CoV-2 pneumonia.

NCT ID: NCT04411901 Completed - Clinical trials for Cystic Fibrosis and Non CF Bronchiectasis

The Role of Vitamin D3 in Pediatric Bronchiectasis Severity

Start date: March 1, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

Vitamin D3 therapy was effective in decreasing the frequency of pulmonary exacerbations and preserving lung functions , thereby improving the disease severity even more in non CF than CF bronchiectasis patients

NCT ID: NCT04271969 Completed - Bronchiectasis Clinical Trials

Clinical Effectiveness Of High Frequency Chest Wall Oscillation (HFCWO) In A Bronchiectasis Population

HFCWO
Start date: February 18, 2020
Phase:
Study type: Observational

The primary objective is to compare the patient's baseline QoL prior to HFCWO use against the patient's QoL at various study timepoints over a one-year period of HFCWO use.

NCT ID: NCT04234789 Completed - Clinical trials for Bronchiectasis Adult

Predictors of Physical Activity Performance and Dynamic Hyperinflation in Patients With Bronchiectasis

Start date: May 2014
Phase: N/A
Study type: Interventional

Bronchiectasis is characterized by abnormal and irreversible airway dilation and can be caused by a wide variety of diseases, including congenital diseases, mechanical bronchial obstruction, respiratory infections, and immunodeficiencies. It is a chronic condition with varying severity. Although some patients remain stable for years, the natural history of the disease is progressive deterioration of lung function, Regarding pulmonary function in this group of patients, there are several changes. In a study of 304 patients with bronchiectasis, spirometry was performed in 274 patients. Most of these patients (46.7%) had an obstructive ventilatory disorder, a small percentage of patients (8%) had restrictive disorder and a portion of patients (23.7%) had mixed disorder. The remaining patients (21.5%) had normal spirometry. Dyspnea in this situation occurs due to neuromechanical dissociation, that is, the respiratory drive is increased, but the inspiratory muscles show a reduction in their ability to produce effective ventilation. Besides not knowing if dynamic hyperinflation (DH) is present in patients with bronchiectasis, the mechanism responsible for its onset is also unknown. Exercise capacity is reduced in many patients with bronchiectasis, but there is little information about the exercise response in this population. The primary objective of this study is to evaluate the prevalence of dynamic hyperinflation in patients with bronchiectasis

NCT ID: NCT04170114 Completed - Cystic Fibrosis Clinical Trials

Comparison of the Efficacy of Comprehensive Respiratory Physiotherapy in Children With Cystic Fibrosis and Non-Cystic Fibrosis Bronchiectasis

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

The effect of comprehensive respiratory physiotherapy applications on respiratory function, functional capacity and peripheral muscle strength in children with cystic fibrosis and non-cystic fibrosis will be compared.

NCT ID: NCT04153448 Completed - Bronchiectasis Clinical Trials

Comparison of Sit-to-stand Test With Six-minute Walk Test in Bronchiectasis and Healthy Children

Start date: December 23, 2019
Phase:
Study type: Observational

Children with bronchiectasis and age-matched healthy controls will be evaluated with sit-to-stand test and six-minute walk test and utilization of STST in determining functional capacity will be investigated.

NCT ID: NCT04122547 Completed - Bronchiectasis Clinical Trials

Efficacy of Roflumilast on Exacerbations in Patients With Non-cystic Fibrosis Bronchiectasis

Start date: January 2015
Phase: Phase 3
Study type: Interventional

Roflumilast compare with placebo for decrease infected exacerbation in non-cystic Bronchiectasis

NCT ID: NCT04122040 Completed - Quality of Life Clinical Trials

Effects of Roxithromycin on Quality of Life and Physiological Outcomes in Bronchiectasis

Start date: March 1, 2011
Phase: Phase 3
Study type: Interventional

roxithormycin 300 mg per day for 12 weeks could improve quality of life and physiological outcomes in bronchiectasis

NCT ID: NCT04085133 Completed - Clinical trials for Pulmonary Tuberculoses

Prevalence and Burden of Bronchiectasis in Tuberculous Patients

Start date: September 26, 2019
Phase:
Study type: Observational [Patient Registry]

Bronchiectasis was described in the early 19th century by Laennec. Bronchiectasis is a chronic condition characterized by permanent and irreversible dilatation of the bronchial airways and impairment of mucociliary transport mechanism due to repeated infection and inflammation leading to colonization of organism and pooling of the mucus in the bronchial tree

NCT ID: NCT04081740 Completed - Asthma Clinical Trials

Biological Determinants of Sputum Rheology in Chronic Airway Diseases

CADRhé
Start date: September 15, 2019
Phase:
Study type: Observational

The primary objective of this study is to investigate the biological determinants of sputum rheology variations.