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Bronchiolitis clinical trials

View clinical trials related to Bronchiolitis.

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NCT ID: NCT02586961 Terminated - Children Clinical Trials

Nebulized Adrenalin and Oral Betamethasone in Children With Bronchiolitis Attending Pediatric Emergencies.

EPIDEX
Start date: October 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The combined administration of high dose of oral betamethasone and nebulization of adrenaline seems to be an attractive therapeutic alternative for reducing the rate of hospitalization for acute bronchiolitis treated in the emergency department. However, it is essential to confirm the trend previously observed with this treatment before using it in current practice.

NCT ID: NCT02585531 Not yet recruiting - Bronchiolitis Clinical Trials

Epinephrine, Dexamethasone and Hypertonic Saline in Bronchiolitis

Start date: November 2015
Phase: Phase 2
Study type: Interventional

Bronchiolitis is one of the main reasons for consultation in primary care and emergency services, as well as the leading cause of hospitalization for lower respiratory tract infection in children under two years. There is still no consensus on the medical management of the disease, in clinical practice there is wide variability in the treatment with inhaled drugs and / or oral bronchodilators, steroids, antihistamines despite the viral etiology of the disease, which results in increased morbidity and a major economic benefit for all health services. Several studies are in relation to the management of bronchiolitis, one of which was made during 2014 in the Naval Hospital of High Specialty which included 90 participants comparing 3 treatment. The treatments administered were: dexamethasone and epinephrine (Levogira) (ED), hypertonic saline 3% (SSH 3%)and saline 0.9% ( SS 0.9%), finding that the handling of ED and SSH 3% had lower rates of hospital admissions compared to the symptomatic management of SS 0.9%. Although the superiority of SSH3% and ED in relation to the use of SS 0.9% was demonstrated, it was not possible to establish difference statistically significant between them. Why it was considered necessary to continue the study focused on determining the difference in the effectiveness of ED and SSH 3%. Therefore, the purpose of this investigation is to determine whether there is a difference between the use of dexamethasone and epinephrine versus hypertonic saline (3%).

NCT ID: NCT02571517 Completed - Clinical trials for Bronchiolitis, Viral

Glucocorticoid Therapy Impact on the Inflammatory Response and Clinical Evolution in Patients With Severe Bronchiolitis

Start date: November 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to to demonstrate that a 7-day course of systemic glucocorticoids decreases the inflammatory activity of moderate or severe bronchiolitis in paediatric patients compared to the standard treatment. To evaluate the morbidity (regarding to the clinical course: Intensive Pediatric Unit Care unit (PICU) admission, mechanical ventilation, ionotropic support, nosocomial infection, rescue therapy for respiratory failure; duration of PICU stay and hospitalization; and exitus) between the treatment and the control groups.

NCT ID: NCT02543073 Recruiting - Clinical trials for Hematopoietic Stem Cell Transplantation

MSC for Treatment of Interstitial Lung Disease After Allo-HSCT

Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Interstitial lung disease (ILD) is the late pulmonary complications after allogeneic hematopoietic stem cell transplantation (allo-HSCT) leading to high morbidity and mortality. At present, the treatment for ILD after allo-HSCT remains in discussion. In this study, the efficacy of mesenchymal stem cells (MSCs) combined azithromycin as well as glucocorticoid as the treatment of ILD will be evaluated in the recipients of allo-HSCT.

NCT ID: NCT02538458 Completed - Bronchiolitis Clinical Trials

Efficacy and Safety of 3% Hypertonic Saline Inhalation (24h vs 72h) to Treat Acute Bronchiolitis in Hospitalized Infants

BRONDUSAL
Start date: November 2014
Phase: Phase 4
Study type: Interventional

Efficacy/Safety of 3% hypertonic saline inhalation (24H vs 72H) to treat acute bronchiolitis in infants.

NCT ID: NCT02495597 Completed - Clinical trials for Bronchiolitis Obliterans

LCI and Bronchial Inflammation in Patients With BO

FRABO-02
Start date: April 2013
Phase: N/A
Study type: Observational

The investigators here compare lung function parameters (RV, RV/TLC and FEF75) with the results of the Lung Clearance index (LCI) . Further this study evaluates bronchial inflammatory markers in 20 patients with bronchiolitis obliterans at the age of 6 to 28 years compared with an age- and sex-matched control group. The investigators will perform a pulmonary function test (body plethysmography with DLCO) and compare the results with the LCI. Further we will measure the fraction of exhaled nitric oxide (FeNO) and draw a blood sample to determine the level of systemic inflammation. Finally induced sputum is collected and a cell count is performed, and cells and supernatants are analyzed for inflammatory markers. This study will set baseline markers for future interventional studies.

NCT ID: NCT02488304 Terminated - Clinical trials for Bronchiolitis Obliterans

Prospective Study for Transplant Optimization Using Functional Imaging (TROFI)

Start date: July 2015
Phase: Phase 2
Study type: Interventional

The objective of this study is to detect BOS in an early stage by using the outcome parameters generated by Functional Respiratory Imaging (FRI). Robust and automated segmentation algorithms will be developed for these parameters, focusing on quantitative computed tomography (CT) image analyses to provide the physician a more sensitive diagnostics tool. The evolution of rejection over time will be monitored using non-rigid image registration methods.

NCT ID: NCT02469597 Recruiting - Bronchiolitis Clinical Trials

Single Dose of Furosemide to Improve Respiratory Distress in Moderate to Severe Bronchiolitis

Start date: October 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess if administration of an early single dose of a diuretic (furosemide) to children with moderate to severe bronchiolitis can reduce extravascular lung water in an effort to reduce respiratory rate, retractions, intubations, and length of stay.

NCT ID: NCT02460614 Completed - Clinical trials for Acute Viral Bronchiolitis

Effects of Rhinopharyngeal Retrograde Clearance in Children With Acute Viral Bronchiolitis

Start date: March 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the immediate effects of retrograde rhinopharyngeal clearance with nasopharyngeal aspiration in children admitted with acute viral bronchiolitis. The investigators selected children, up to 12 months old, admitted for acute viral bronchiolitis. Patients were divided in aspiration group (AG), submitted to nasopharyngeal aspiration, and clearance group (CG), submitted to retrograde rhinopharyngeal clearance with physiological solution (0.9%) instillation (RRC) technique. In both groups children were evaluated three times in the same day in order to verify cardiorespiratory parameters, clinical score of respiratory dysfunction and adverse effects.

NCT ID: NCT02458300 Completed - Bronchiolitis Clinical Trials

Clinical Evaluation of the Response to Chest Physiotherapy in Children With Acute Bronchiolitis

FIBARRIX
Start date: January 2015
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the clinical response of children diagnosed with acute bronchiolitis, relative to a chest physiotherapy protocol. Comparing this treatment with standard care of the nursing staff and auxiliaries of infants patients aged 1 month to 2 years.