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Bronchiolitis, Viral clinical trials

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NCT ID: NCT01189149 Completed - Viral Bronchiolitis Clinical Trials

Intravenous Fluids Versus Naso/Orogastric-tube Feeding in Hospitalized Infants With Bronchiolitis

Start date: December 2008
Phase: N/A
Study type: Interventional

Oro- or nasogastric tube feeding is safe and may be more physiologic than intravenous (IV) fluids in hospitalized infants with acute viral bronchiolitis.

NCT ID: NCT01120496 Completed - Bronchiolitis Clinical Trials

Nebulized Hypertonic Saline Treatment in Hospitalized Children With Moderate to Severe Viral Bronchiolitis

Start date: November 2008
Phase: N/A
Study type: Interventional

The purpose of this study is planned to investigate whether frequently inhaled hypertonic saline (HS) can relieve symptoms and signs faster than normal saline (NS) and shorten length of stay (LOS) significantly for moderately to severely ill infants with bronchiolitis without apparent adverse effects.

NCT ID: NCT01091064 Withdrawn - Bronchiolitis Clinical Trials

Impact Of A Health Care Protocol For Patients Suffering Symptoms Of Mild Acute Viral Bronchiolitis On Early Release In The Emergency Department

Start date: October 2011
Phase: Phase 2
Study type: Interventional

Acute viral bronchiolitis is the principal cause of lower respiratory tract infection in infants worldwide. It is characterized by a first episode of respiratory distress preceded by rhinorrhea, cough and fever. The majority of patients present with mild symptoms which can be treated safely at home by parents. Every year between October thru April emergency departments in North America are overwhelmed with patients waiting to be seen with mild respiratory infections, such as bronchiolitis. Thus new strategies in health care have to be elaborated to reduce costs and waiting time in the emergency department. The investigators hypothesize that patients liberated from triage with mild acute viral bronchiolitis would have the same rate of office re-visits than those with mild acute bronchiolitis in the emergency department.

NCT ID: NCT00884429 Completed - Viral Bronchiolitis Clinical Trials

Effectiveness of Chest Physiotherapy in Infants With Acute Viral Bronchiolitis

ECPAVB
Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to verify the effectiveness of chest physiotherapy (actual versus conventional) on respiratory distress in infants with acute viral bronchiolitis.

NCT ID: NCT00729274 Withdrawn - Clinical trials for Acute Viral Bronchiolitis.

HYPERTONIC SALINE IN ACUTE VIRAL BRONCHIOLITIS: A RANDOMIZED CLINICAL TRIAL

Start date: November 2011
Phase: N/A
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 (placebo). We hypothesise that patients with bronchiolitis who receive nebulized hypertonic saline solution will have less respiratory distress, less duration of symptoms and therefore less risk of being hospitalized than those receiving normal saline solution.

NCT ID: NCT00677729 Completed - Viral Bronchiolitis Clinical Trials

Hypertonic Saline to Reduce Hospital Admissions in Bronchiolitis

Start date: November 2008
Phase: Phase 2
Study type: Interventional

Inhaled 3% hypertonic saline (HS) administered every 2-8 hours to infants admitted to hospital with viral bronchiolitis has been shown to improve airway clearance and reduces length of stay. Hypothesis: When infants first present to the ER, frequent administration of HS over a brief time period will provide significant symptom improvement such that the need for hospital admission will be reduced. Objective: To determine in a randomized, controlled and double-blind fashion if the short term intensive use of inhaled 3% hypertonic saline (HS) in the Emergency Room (ER) can reduce the rate of hospital admission for infants presenting with moderately severe viral bronchiolitis.

NCT ID: NCT00261937 Completed - Bronchiolitis Clinical Trials

Inhaled Furosemide Versus Placebo for Acute Viral Bronchiolitis in Hospitalized Infants

Start date: December 2005
Phase: Phase 1
Study type: Interventional

We hypothesize that inhaled Furosemide will be an effective treatment in infants with acute bronchiolitis.

NCT ID: NCT00125450 Completed - Viral Bronchiolitis Clinical Trials

Evaluation of Chest Physiotherapy for Acute Bronchiolitis in Toddlers (BRONKINOU)

BRONKINOU
Start date: September 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether chest physiotherapy with forced expiratory technique reduces delay of healing in acute bronchiolitis of children between 15 days and 24 months of age.

NCT ID: NCT00122785 Completed - Clinical trials for Bronchiolitis, Viral

Single Injection of Dexamethasone for Acute Bronchiolitis in Young Children

Start date: April 2002
Phase: N/A
Study type: Interventional

The purpose of this study was to determine whether a single intramuscular injection of dexamethasone decreased the duration of symptoms of acute bronchiolitis in young children.

NCT ID: NCT00119002 Completed - Clinical trials for Bronchiolitis, Viral

The Effectiveness of Oral Dexamethasone for Acute Bronchiolitis

Start date: January 2004
Phase: Phase 4
Study type: Interventional

This study will compare a single dose of oral dexamethasone to placebo in a multicenter, randomized, double blind trial of infants aged 2 to 12 months with first-time bronchiolitis (defined as wheezing within 7 days of onset). This is given as additional therapy beyond any other routine therapy used at that center. No current standard therapy is withheld, and no additional tests or other treatments are part of the study.The primary hypothesis is that dexamethasone will be more effective than placebo in preventing hospital admission. The secondary hypotheses are that dexamethasone will decrease respiratory scores and possibly the duration of the disease when compared to placebo, and that dexamethasone will be as safe and as well tolerated as placebo.