Clinical Trials Logo

Wheezing clinical trials

View clinical trials related to Wheezing.

Filter by:

NCT ID: NCT02269761 Terminated - Dyspnea Clinical Trials

Chest Ultrasound of ER Patients With Cough or SOB

Start date: September 2014
Phase:
Study type: Observational

Acute dyspnea (shortness of breath) is a common complaint for patients presenting to the Emergency Department (ED). The chest radiograph (CXR) has been the mainstay in evaluating patients with shortness of breath and often provides the timely diagnosis of pneumonia, pneumothorax, pulmonary edema, among other primary diseases of the lung. There are limitations with chest radiograph such as large body mass (e.g, obesity) and patient positioning. On occasion, chest radiography findings are difficult to interpret. Lung ultrasonography may offer a means of clarifying ambiguous results. The objective of this study to determine the usefulness of point of care lung ultrasound in evaluating patients presenting to the ED with shortness of breath, cough and/or wheezing.

NCT ID: NCT02233985 Recruiting - Bronchiolitis Clinical Trials

Nebulized 3% Hypertonic Saline Solution Treatment of Bronchiolitis in Infants

Start date: August 2013
Phase: Phase 4
Study type: Interventional

- Determine the efficacy of nebulized salbutamol/hypertonic saline combination in moderate to severe bronchiolitis.

NCT ID: NCT02163096 Completed - Asthma Clinical Trials

A Study to Assess Benign Joint Hypermobility Syndrome in Children With a History of Wheezing or Asthma

Start date: June 2014
Phase: N/A
Study type: Observational

The purpose of this study is to assess benign joint hypermobility syndrome (BJHS) in children with a history of wheezing or asthma. BJHS is a common syndrome of joint and connective tissue laxity without any other rheumatologic disease. This assessment will be performed by using either method below depending upon if the child has a history of wheezing or severe asthma: 1. Determine the correlation, if there is an increased rate of BJHS in children with a history of wheezing as well as if there is an increased history of wheezing in children with BJHS; or 2. Determine asthma control, lung function and asthma exacerbations (a flare up or acute worsening of symptoms) in children with BJHS compared to children with asthma without BJHS, to assess if it BJHS is associated more with children with severe asthma.

NCT ID: NCT02148796 Active, not recruiting - Asthma Clinical Trials

Oral Bacterial Extract for the Prevention of Wheezing Lower Respiratory Tract Illness

ORBEX
Start date: January 3, 2017
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate if Broncho-Vaxom® given to high risk infants for 10 days, monthly, for two consecutive years can increase time to occurrence of the first episode of wheezing lower respiratory tract illness (WLRI) during a three year observation period off therapy.

NCT ID: NCT02113072 Completed - Clinical trials for Respiratory Tract Diseases

Recurrent Wheezing in Infants: Risk Factors and Prevention With Probiotics.

Start date: April 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate whether Probiotics promote reduction of recurrent wheezing in infants, stimulating the immune system to Th1 response.

NCT ID: NCT01861548 Completed - Asthma Clinical Trials

Polish Mother and Child Cohort Study (REPRO_PL) - Follow up of the Children.

REPRO_PL
Start date: January 2007
Phase: N/A
Study type: Observational

The Polish Mother and Child Cohort is multicentre prospective study on different exposures. Prospective cohort study design enables identification of exposures that may influence pregnancy outcome and chil-dren's health, verification of such exposures by biomarker measurements and notification of any changes in exposure levels. The aim of the study is to evaluate the impact of exposure to different environmental factors during pregnancy and after birth on pregnancy outcome and children's health. Specific research hypotheses refer to the role of heavy metals, exposure to polycyclic aromatic hydrocar-bons (PAHs) and environmental tobacco smoke (ETS) in the aetiology of intrauterine growth retardation (IUGR), preterm delivery (PD) and the risk of respiratory diseases, allergy and poor mental and physical development. It is also intended to explain the role of oxidative stress and nutritional status of the pregnant women. The impact of occupational exposures and stressful situations on pregnancy outcome will be evaluated from question-naire data. The results of the study will help to determine levels of child prenatal and postnatal exposure in several areas of Poland and their im-pact on course and outcome of pregnancy and children's health. This protocol concerns the children that are followed-up from birth to the age of 2 years to determine long term effects of pre- and postnatal environmental exposures.

NCT ID: NCT01606319 Completed - Asthma Clinical Trials

Acetaminophen Versus Ibuprofen in Children With Asthma

AVICA
Start date: February 2013
Phase: Phase 3
Study type: Interventional

The Acetaminophen Versus Ibuprofen in Children with Asthma study will test the primary hypothesis that in preschool children 12-59 months of age with persistent asthma on standardized asthma therapy, the number of asthma exacerbations requiring systemic corticosteroids will be more frequent in children randomized to receive acetaminophen as compared to those randomized to receive ibuprofen on an as needed basis for fevers and pain.

NCT ID: NCT01606306 Completed - Asthma Clinical Trials

Individualized Therapy For Asthma in Toddlers

INFANT
Start date: February 2013
Phase: Phase 3
Study type: Interventional

The INFANT study will test whether, in preschool children 12-59 months of age with persistent asthma, the following Step 2 asthma therapies will provide similar degrees of asthma control: 1. Daily inhaled corticosteroid (ICS) treatment, 2. Daily leukotriene receptor antagonist (LTRA) treatment, and 3. As-needed ICS plus short-acting beta agonist (as-needed ICS/SABA) rescue treatment.

NCT ID: NCT01601847 Completed - Allergy Clinical Trials

Wheezing in Black Preterm Infants: Impact of Vitamin D Supplementation Strategy

D-Wheeze
Start date: January 2013
Phase: Phase 4
Study type: Interventional

The goal of this study is to identify a vitamin D supplementation strategy that best promotes the lung, immune, and overall health of black infants born preterm (28-36 weeks gestational age). This is a high risk population that seems to have unique vitamin D needs, and inappropriate supplementation may promote wheezing or allergy. The results of this study will help form nutritional recommendations for the approximately 100,000 black infants born at 30-36 weeks gestational age in the U.S. every year.

NCT ID: NCT01452945 Completed - Bronchiolitis Clinical Trials

Bedside Lung Ultrasound in Young Children Presenting to the Emergency Department (ED) With Wheezing

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

Young children presenting to the Emergency Department (ED) with wheezing often have prolonged stays in the ED or even get admitted to the hospital. This is a prospective observational study in which the investigators will use bedside 2D ultrasound to evaluate the lung ultrasound findings in children less than 24 months presenting to the ED with wheezing. The investigators hypothesize that children less than 24 months presenting to the Emergency Department with wheezing will have a range of lung ultrasound findings that will include normal findings, B lines, subpleural consolidations, and pleural effusions. The investigators also hypothesize that the findings will be reproducible between two equally trained providers. The investigators also hypothesize that lung ultrasound findings patients 0-24 months presenting to the ED with wheezing will correlate with specific clinical outcomes. An exploratory analysis will be performed to look for correlations between lung US findings and acute severity, final diagnosis, presenting symptoms, prematurity, risk factors for atopy, response to treatment and radiologic or viral studies if performed.