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Bronchiolitis clinical trials

View clinical trials related to Bronchiolitis.

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NCT ID: NCT01016249 Completed - Bronchiolitis Clinical Trials

Nebulized 5% Hypertonic Saline for the Treatment of Bronchiolitis

Start date: April 2007
Phase: Phase 4
Study type: Interventional

The investigators reasoned that a hypertonic saline concentration higher than 3% could be safe and more efficacious in the treatment of bronchiolitis, alleviating severe symptoms and preventing the need for hospitalization in some instances.

NCT ID: NCT01014910 Completed - Hypoxia Clinical Trials

Intermittent Versus Continuous Pulse Oximetry Monitoring of Infants Admitted for Bronchiolitis

Start date: December 2009
Phase: N/A
Study type: Interventional

Bronchiolitis is a lower respiratory tract infection (LRTI) syndrome cause by different types of viruses and occurs in young children. Although bronchiolitis is a widespread and fairly common illness in children, pediatricians vary significantly in how it is treated. This includes how children are monitored for their oxygen status when not receiving supplemental oxygen. Studies suggest that continuous pulse oximetry measurement of children admitted to the hospital with bronchiolitis regardless of use of supplemental oxygen prolongs their hospital stay. This increases the cost of care for these patients and increases their risk of hospital-associated complications. This study is a randomized trial of continuous pulse oximeter use in patients admitted with bronchiolitis versus transitioning patients not requiring oxygen to intermittent pulse oximetry monitoring. The investigators hypothesize that this will decrease length of stay as well as associated costs of care and number of medical interventions performed in the hospital.

NCT ID: NCT01009619 Completed - Graft Rejection Clinical Trials

Azithromycin in Bronchiolitis Obliterans Syndrome

AZI001
Start date: September 2005
Phase: Phase 4
Study type: Interventional

Preventive treatment with azithromycin reduces the prevalence fo Bronchiolitis Obliterans Syndrome after lung transplantation.

NCT ID: NCT00891865 Completed - Clinical trials for Bronchiolitis Obliterans

Viral Triggers in Pediatric Lung Transplantation

Start date: June 2009
Phase:
Study type: Observational

The purpose of this study is to determine whether respiratory viral infections increase the risk of bronchiolitis obliterans syndrome (BOS), obliterative bronchiolitis (OB), death, or retransplantation in children who have received lung transplants.

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: NCT00863317 Completed - Bronchiolitis Clinical Trials

Trial of Montelukast for Treatment of Acute Bronchiolitis

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

The primary rationale for this study is to evaluate the effect of once daily montelukast on duration of acute illness in infants with first-time bronchiolitis.

NCT ID: NCT00861900 Completed - Clinical trials for Bronchiolitis Obliterans

Immune Mechanisms of Rejection in Human Lung Allografts

Start date: January 1998
Phase:
Study type: Observational

The investigators have obtained compelling evidence that the development of anti-human leukocyte antigen (anti-HLA) antibodies against mismatched donor antigens significantly correlates with the development of bronchiolitis obliterans (BOS). Further, these anti-HLA antibodies are developed at least 15 months prior to any clinical evidence of BOS. This lag period between the development of anti-HLA antibodies and the onset of BOS gives us an opportunity to intervene to delay and/or prevent the development of BOS.

NCT ID: NCT00755781 Completed - Lung Transplant Clinical Trials

Study of Cyclosporine Inhalation Solution (CIS) in Improving Bronchiolitis Obliterans Syndrome-Free Survival Following Lung Transplantation

CIS001
Start date: September 2008
Phase: Phase 3
Study type: Interventional

A Phase III, multi-center, randomized, controlled study designed to demonstrate the efficacy and safety of Cyclosporine Inhalation Solution (CIS)in improving survival and preventing bronchiolitis obliterans syndrome (BOS) when given prophylactically to lung transplant recipients in addition to their standard immunosuppressive regimen.

NCT ID: NCT00743171 Completed - Death Clinical Trials

Long-Term Study On Home Spirometry After Lung Transplantation

Start date: January 2000
Phase: N/A
Study type: Observational

Prospective cohort, mono-center study included electronic data of home spirometry (HS, lung function) of lung transplant recipients

NCT ID: NCT00701922 Completed - Clinical trials for Lung Transplantation

Surveillance Study of Viral Infections Following Lung Transplantation

Start date: October 2005
Phase: N/A
Study type: Observational

The present study was conducted to study the impact community acquired respiratory virus (CARV) infections in an outpatient setting on graft function of lung transplant recipients. The study was aimed to identify risk factors for CARV infections. The study was further intended to investigate an association of Epstein-Barr virus (EBV), cytomegalovirus (CMV) and human adenovirus (HAdV) with the development of BOS and to identify risk factors for virus detection in blood.