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Bronchiolitis clinical trials

View clinical trials related to Bronchiolitis.

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NCT ID: NCT00188825 Completed - COPD Clinical Trials

Study Comparing Simulect Plus Standard Immunosuppression to Standard Immunosuppression Alone for the Prevention of Acute Rejection and Bronchiolitis Obliterans in Lung Transplant

Start date: May 2004
Phase: Phase 3
Study type: Interventional

The study will evaluate the efficacy and safety of basiliximab Vs placebo as induction therapy combined with standard triple immunosuppression therapy, in the prevention of acute rejection episodes and prevention of Bronchiolitis Obliterans Syndrome.

NCT ID: NCT00151905 Completed - Bronchiolitis Clinical Trials

The Use of an Inhaled Salt Solution to Treat Viral Lung Infections in Infants.

Start date: November 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Bronchiolitis is a common viral lung infection in infants. Standard treatment often includes the use of inhaled medications which are usually first mixed with a standard salt solution. Inhalation of a more concentrated salt solution (hypertonic saline) has been successfully used to treat other types of lung disease in children and adults. The purpose of this study is to see if using inhaled hypertonic saline helps infants with bronchiolitis get better more quickly.

NCT ID: NCT00141726 Completed - Clinical trials for Respiratory Distress Syndrome, Adult

Study of Enbrel (Etanercept) for the Treatment Sub-Acute Pulmonary Dysfunction After Allogeneic Stem Cell Transplant

Start date: October 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effectiveness of etanercept in the treatment of patients with sub-acute lung injury following a bone marrow transplant. This study will also examine the toxicity of treatment with etanercept as well as whether there is an improved quality of life in these patients.

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.

NCT ID: NCT00116584 Completed - Bronchiolitis Clinical Trials

Heliox-Driven Racemic Epinephrine in Treatment of Bronchiolitis in Pediatric ED Patients

Start date: December 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess whether children with moderate to severe bronchiolitis treated with standard racemic epinephrine therapy via 70:30 helium-oxygen (heliox) driven nebulization will have improvements in measurements of airway more rapidly than those treated with conventional air-oxygen driven nebulization.

NCT ID: NCT00076973 Completed - Bronchiolitis Clinical Trials

An Investigational Drug Study to Treat Respiratory Symptoms Associated With Respiratory Syncytial Virus (RSV) Bronchiolitis (0476-272)

Start date: August 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to look at whether an investigational drug can treat the breathing symptoms of RSV bronchiolitis in children 3 to 24 months of age.

NCT ID: NCT00029328 Completed - Pneumonia Clinical Trials

Etanercept for Non-Infectious Lung Injury Following Bone Marrow Transplantation

Start date: September 2001
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the effects of etanercept, and define the toxicity, when administered to patients with acute non-infectious lung injury (idiopathic pneumonia syndrome, IPS) and with subacute pulmonary dysfunction after allogeneic stem cell transplantation.

NCT ID: NCT00027235 Completed - Clinical trials for Lung Diseases, Interstitial

Popcorn Lung: the Discovery of a New Disease

Start date: n/a
Phase: N/A
Study type: Observational

Recently, an epidemic of pulmonary disease has been recognized among workers in a popcorn factory in Jasper, Missouri. The exposure agent has not yet been identified, but suspects include butter flavoring and the powdered salt used in the mixing room. This disease resembles "Bronchiolitis Obliterans Syndrome", an illness that makes it difficult to breathe. Of the 117 workers studied, one year later, 25 subjects whom were working in the mixing room or in the microwave packaging area have had decreases in lung function seven times the norm for their age. Industrial hygiene experts revealed that dust concentrations of salt and other flavorings were much higher in the mixing room compared to the office and outdoor work areas. Recently, rats were exposed to vapors created by heating the butter flavor compound obtained from this plant. Six-hour exposure to vapors at very high concentration resulted in significant damage to the breathing apparatus. Thus, there is clinical, epidemiological, and animal toxicity data that appears to implicate some constituent present during the mixing of the butter flavoring, salt, and oil causing a form of obstructive airway disease that has been rapidly progressive in a number of workers. It is not clear what the pathophysiologic nature of this entity is, though it resembles Bronchiolitis Obliterans Syndrome. It is not known what the long term consequence of this will be on the active workers, nor is it clear whether preventive measures taken to reduce exposures in the mixing room and elsewhere in the plant are going to be effective.