Clinical Trials Logo

Bronchiolitis clinical trials

View clinical trials related to Bronchiolitis.

Filter by:

NCT ID: NCT02316392 Completed - Clinical trials for Bronchiolitis Obliterans Syndrome

Imaging and Understanding BOS in Lung Transplantation

Start date: December 2014
Phase:
Study type: Observational

This study is a prospective, non-randomized, longitudinal, observational study that will recruit about 5 lung transplant patients per year for 3 years.

NCT ID: NCT02262299 Completed - Clinical trials for Disorder Related to Lung Transplantation

European Trial of Pirfenidone in BOS, A European Multi-center Study

EPOS
Start date: May 2015
Phase: Phase 2/Phase 3
Study type: Interventional

A European multi-centre, randomised, double-blind placebo-controlled trial of Pirfenidone in bronchiolitis-obliterans-syndrome grade 1-3 in lung transplant recipients. Randomized double blinded, placebo controlled study. Eligible patients are to be randomized in a 1:1 ratio to receive either Pirfenidone 2403 mg/d or the matching placebo treatment for 6 months. Primary objective To evaluate the effect of Pirfenidone on the change in FEV1 in liters over 6 months in lung transplant recipients with bronchiolitis obliterans syndrome.

NCT ID: NCT02181712 Completed - Clinical trials for Bronchiolitis Obliterans

Mesenchymal Stem Cell Therapy for Lung Rejection

Start date: July 2014
Phase: Phase 1
Study type: Interventional

To assess the safety and feasibility of mesenchymal stem cells therapy in patients with transplant related bronchiolitis obliteran syndrome (BOS)

NCT ID: NCT02162745 Completed - Bronchiolitis Clinical Trials

Nasal Irrigation in Infants With Bronchiolitis.

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

Bronchiolitis is a leading cause of acute illness and hospitalization in the first year of life. Most children with bronchiolitis have mild disease and are managed at home with support from primary care providers, while children with more severe symptoms require supportive therapy with oxygen and fluid administration. Neonates may be obligate nasal breathers until they are at least 2 months old and nasal obstruction may play a relevant role in respiratory resistances throughout the first months of life, whereas nasal passages may exhibit as much as 50% of the total airway resistance. Some guidelines recommend to clear the nostrils of secretions to improve airway patency but no controlled trial on the efficacy of nasal irrigation in infants with bronchiolitis was carried out. The aim of this randomized controlled trial is to compare normal saline and hypertonic solution for nasal irrigation versus simple supportive care in infants admitted to Emergency Department with bronchiolitis and mild desaturation.

NCT ID: NCT02145520 Completed - Bronchiolitis Clinical Trials

Efficacy of Magnesium Sulfate in the Treatment of Bronchiolitis

Start date: October 2012
Phase: Phase 2
Study type: Interventional

In this study, investigators will compare the efficacy and safety of intravenous (IV) Magnesium sulfate in decreasing bronchiolitis clinical severity score and the duration of hospitalization in admitted patients, as compared to placebo.

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: NCT02094664 Completed - Bronchiolitis Clinical Trials

Heated Humidified Oxygen Compared to Dry Oxygen Therapy in Children With Bronchiolitis

Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare heat and humidified oxygen with cold and dry oxygen in children with bronchiolitis. The hypotheses are that heating and humidifying inspired low flow supplemental oxygen will optimize mucociliary function thereby, 1) improve oxygenation, 2) decrease work of breathing, and 3) decrease length of hospital stay.

NCT ID: NCT02036970 Completed - Clinical trials for Pulmonary Hypertension

Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT

Start date: May 31, 2014
Phase: Phase 2
Study type: Interventional

This study assesses the safety and efficacy of bardoxolone methyl relative to placebo in patients with pulmonary hypertension to determine the recommended dose range, evaluate the change from baseline in 6-minute walk distance (6MWD) and determine the effect of Bardoxolone methyl in pulmonary hypertension associated with connective tissue disease, interstitial lung disease, and idiopathic etiologies, including subsets of patients with WHO Group III or WHO Group V PH following 16 weeks of study participation.

NCT ID: NCT02032381 Completed - Clinical trials for Bronchiolitis Obliterans

Prospective Study of Belated Pulmonary Complications Occurring in Children Treated With Allogeneic Hematopoietic Stem Cells.

RESPPEDHEM
Start date: January 2014
Phase: N/A
Study type: Interventional

Hematopoietic stem cell transplantation (HSCT) is used to treat an expanding array of malignant and non-malignant disorders. This is a prospective multicenter study, in pediatric allo-BMT recipients to analyze the spectrum of noninfectious pulmonary complications (PC), to evaluate the prevalence and course of PFT abnormalities before and after transplant, and to detect risk factor for PC.

NCT ID: NCT02029040 Completed - Acute Bronchiolitis Clinical Trials

Nebulized 3% Hypertonic Saline in the Treatment of Acute Bronchiolitis

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

This is a randomized, double-blind, controlled trial in the Pediatric Emergency Department. The primary objective is to determine whether nebulized 3% hypertonic saline is more effective than nebulized 0.9% saline in the treatment of bronchiolitis in the emergency department.