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Bronchiolitis, Viral clinical trials

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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: NCT02126748 Completed - Bronchiolitis Clinical Trials

The Effectiveness of AAD and IPV to Treat Hospitalized Infants (<2years) With Acute Viral Bronchiolitis.

Start date: December 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effectiveness of two airway clearance techniques; Intrapulmonary Percussive Ventilation and Assisted Autogenic Drainage in hospitalized infants under the age of 2 with acute viral bronchiolitis.

NCT ID: NCT02045238 Terminated - Bronchiolitis Clinical Trials

Inhaled Hypertonic Saline Use in the Emergency Department to Treat Acute Viral Bronchiolitis

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

Acute viral bronchiolitis is an extremely common childhood disease, responsible for approximately 17% of childhood admissions to hospital per year, with an annually cost that reaches U$ 500 million. Despite being a well known disease among pediatricians, there are few, if any, effective treatment options apart from oxygen supplementation and adequate hydration. The purpose of this study is to determine wether nebulized hypertonic saline (3%) is more effective than normal saline (0,9%) when used in repeated doses during the first 24 hours of in-hospital treatment.

NCT ID: NCT01873144 Completed - Clinical trials for Acute Viral Bronchiolitis

High Flow Therapy vs Hypertonic Saline in Bronchiolitis

Start date: October 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate that heated, humidified, high-flow nasal cannula (HHHFNC) is superior to hypertonic saline solution (HSS) in the treatment of moderate acute viral bronchiolitis in infants in improving respiratory distress and comfort and reducing length of hospital stay (LOS) and admission to Pediatric Intensive Care Unit (PICU).

NCT ID: NCT01777347 Completed - Clinical trials for Acute Viral Bronchiolitis

Efficacy of 3% Hypertonic Saline in Acute Viral Bronchiolitis

GUERANDE
Start date: October 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether nebulized hypertonic saline solution reduces the admission rate 48 hours after initial treatment in the emergency department, when compared to normal saline solution (control).

NCT ID: NCT01618175 Not yet recruiting - Clinical trials for Bronchiolitis, Viral

Home Oxygen Treatment of Childhood Acute Bronchiolitis

Start date: October 2012
Phase: N/A
Study type: Interventional

Background: acute bronchiolitis (AB) is a common reason for hospitalization of infants in all population groups, and is usually due to respiratory syncytial virus (RSV) infection. The main cause for hospitalization is often a need for oxygen, but can also include high fever (with a suspected secondary bacterial infection) or increasing respiratory distress. In a minority of cases (some of which can be identified in advance by defining risk groups) a serious illness may develop, including risk of respiratory failure and death. Most cases will just require supplemental oxygen and suction of secretions from the nose (as listed in the recommendations of the American Academy of Pediatrics - AAP). However, this apparently "simple" treatment still requires continued hospitalization. This results in a sharp increase in bed occupancy in Israeli hospital pediatric departments in the winter months. In recent years two studies from developed countries have been published where safety has been demonstrated for home oxygen treatment for babies with AB. However, feasibility studies have not been published yet, for example for populations living in poor conditions. The General Health Services (Klalit) in Israel provides integrated hospital and community health service to the majority of the population living o in our region, thus presenting an opportunity for optimal interventions related to this disease.

NCT ID: NCT01437956 Not yet recruiting - Clinical trials for Acute Viral Bronchiolitis

KL-6 Protein as a Biomarker of Lung Injury in Viral Bronchiolitis

Start date: October 2011
Phase: N/A
Study type: Observational

Serum KL-6 protein has been described as a biomarker of epithelial lung injury in Respiratory Syncytial Virus bronchiolitis. The investigators can imagine that epithelial injury intensity has consequences on immediate and later respiratory prognosis. Furthermore, this prognosis seems to be different according to the respiratory causative virus. The investigators propose to study, during an epidemic season, the correlation between KL-6 levels and clinical severity, and the type of viral infection.

NCT ID: NCT01354561 Completed - Viral Bronchiolitis Clinical Trials

Respiratory Physical Therapy on the Cardiac Autonomic Modulation Paediatric Patients

Start date: February 2007
Phase: N/A
Study type: Interventional

The present study investigated the influence of respiratory affections on the heart rate variability (HRV) of paediatric patients. We have hypothesised that respiratory physiotherapy would promote a beneficial effect on the cardiac autonomic modulation. Twenty-four children, who were divided into respiratory disease group (RG) and control (CG) groups, were studied. Analysis of HRV was performed with the RG in the dorsal decubitus position during four different moments: basal record (30 minutes); 5 minutes after respiratory physiotherapy by means of airway clearance techniques (10-minute record); 5 minutes after nasotracheal suction (10-minute record); and 40 minutes after nasotracheal suction (30-minute record). CG group was submitted to the same protocol, except nasotracheal suction, which was not performed due to ethical reasons.

NCT ID: NCT01295398 Active, not recruiting - Clinical trials for Acute Viral Bronchiolitis

Influence of the Nebulizer on the Clinical Efficacy of Hypertonic Saline 3% in Children Aged Less Than 18 Months and Hospitalized With Acute Viral Bronchiolitis

Start date: December 2010
Phase: N/A
Study type: Interventional

The aim of the investigators study is to compare in children aged less than 18 months and hospitalized for an acute viral bronchiolitis the efficacy of the HS 3% (Mucoclear®, sterile ampoules of 4 ml) nebulised with a conventional jet-nebulizer (particles diameter of 4-5 µm), or with a jet-nebulizer adapted for infants (particles diameter of 2-2.5 µm), or with a mesh-nebulizer adapted for infants (particles diameter of 2-2.5 µm).

NCT ID: NCT01247064 Completed - Clinical trials for Bronchiolitis, Viral

Hypertonic Saline for Acute Bronchiolitis

Start date: October 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether nebulized 3% hypertonic saline (HS) improves respiratory distress in children 2-23 months presenting to the emergency department (ED) with acute bronchiolitis with persistent respiratory distress after initial therapy with a trial of nebulized albuterol.