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Asthma clinical trials

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NCT ID: NCT02498834 Completed - Asthma Clinical Trials

Using Question Prompt Lists During Pediatric Asthma Visits to Increase Adolescent Involvement

Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to conduct a randomized controlled trial with English and Spanish-speaking adolescents to compare the effectiveness of an adolescent "asthma question prompt list" with a supportive educational video intervention with usual care. The hypothesis of this study is that by showing the parents and adolescents the educational video and then providing the adolescents with the one-page "asthma question prompt lists" to use during their visits will improve: (a) asthma control, (b) adolescent self-efficacy in managing asthma, and (c) adolescent quality-of-life.

NCT ID: NCT02497222 Withdrawn - Asthma Clinical Trials

Pilot Study of RNS60 in Allergen-induced Bronchoconstriction

Start date: n/a
Phase: Phase 2
Study type: Interventional

This study evaluates the use of RNS60 in the treatment of asthma examining regional improvements in inflammation using PET imaging. All subjects will be treated with both RNS60 and placebo in a crossover design.

NCT ID: NCT02496715 Withdrawn - Asthma Clinical Trials

Randomized, Placebo-controlled Study Comparing Efficacy of Fluticasone/Salmeterol Combination to Advair in Asthmatics

Start date: September 2015
Phase: Phase 3
Study type: Interventional

This is a pivotal trial that will examine therapeutic equivalence (BE) of a new generic fixed-dose combination product containing fluticasone propionate 100 mcg / salmeterol 50 mcg (as xinafoate salt) and reference listed drug (RLD) Advair® Diskus 100/50 in adult patients with chronic but stable asthma as defined in the National Asthma Education and Prevention Program Expert Panel Report 3 (NAEPP 3) guidelines

NCT ID: NCT02496468 Recruiting - Asthma Clinical Trials

Pediatric Arm of DZL All Age Asthma Cohort

ALLIANCE
Start date: January 2013
Phase:
Study type: Observational

Despite its common occurrence, still little is known about pathomechanisms determining different wheeze and asthma trajectories and phenotypes in children, and those beginning in adulthood. Therefore, deciphering underlying determinants for different childhood and adult asthma phenotypes is urgently needed to develop personalized treatment approaches targeting distinct underlying mechanisms. Thereby, secondary prevention early in the disease process can also be achieved. The decoding of such mechanisms and their translation to the individual patient is the aim of the Disease Area Asthma Allergy of the 'German Centre for Lung Research' (DZL).

NCT ID: NCT02495168 Completed - Asthma Clinical Trials

Randomized, Placebo-Controlled, Multidose, Study Comparing Generic Budesonide/Formoterol Fumarate Dihydrate to Symbicort® in Asthmatic Participants

Start date: January 13, 2017
Phase: Phase 3
Study type: Interventional

This study has a randomized multiple-dose, placebo-controlled, parallel group design consisting of a 2-week open placebo Run-in Period followed by a 6-week Treatment Period with placebo, test product (budesonide 80 microgram [μg]/formoterol fumarate dihydrate 4.5 μg), or reference product (Symbicort® inhalation aerosol).

NCT ID: NCT02494076 Completed - Asthma Clinical Trials

Positive Expiratory Pressure for the Treatment of Acute Asthma in Children

Start date: October 2014
Phase: Phase 4
Study type: Interventional

Asthma is a leading cause of emergency department (ED) visits for children. A novel way of treating asthma is the use of positive expiratory pressure (PEP). Positive expiratory pressure works by creating pressure in the lungs to keep airways open and to clear mucus from the lungs. PEP is already used in the treatment of asthma at the investigators institution, but studies evaluating the efficacy of PEP therapy in asthma exacerbations do not exist. This study plans to learn more about the use of PEP therapy in the treatment of asthma exacerbations in children in the emergency department. Specifically, the study aims to evaluate if PEP therapy reduces the severity of asthma exacerbations in children and if it reduces the need for additional therapies and admission to the hospital. This study will be a randomized control trial comparing children who receive standard therapy to those who receive standard therapy plus PEP therapy in the treatment of asthma exacerbations. Children age 2 to 18 years presenting to the ED with moderate to severe asthma exacerbations will be included in the study. Reduction in clinical asthma severity will be measured by change in the Pulmonary Asthma Score (the respiratory severity score used at the investigators institution). The need for additional therapies and hospitalization will also be evaluated.

NCT ID: NCT02491970 Terminated - Asthma Clinical Trials

Small Airway Function of Fluticasone/Formoterol (Flutiform®) and Fluticasone/Salmeterol

RECONFFIRM
Start date: August 31, 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to demonstrate superiority of Fluticasone/Formoterol (Flutiform®) to Fluticasone/salmeterol based on the small airway function by assessing the Impulse Oscillometic System (IOS) in uncontrolled asthma patients requiring ICS/LABA concomitant treatment.

NCT ID: NCT02491684 Completed - Asthma Clinical Trials

A Study in Asthma Patients to Evaluate Efficacy, Safety and Tolerability of 14 Days Once Daily Inhaled Interferon Beta-1a After the Onset of Symptoms of an Upper Respiratory Tract Infection

INEXAS
Start date: July 21, 2015
Phase: Phase 2
Study type: Interventional

A study to investigate if inhaled Interferon beta-1a is safe and tolerated, and can prevent or reduce the severity of asthma attacks when administered to asthma patients at the onset of symptoms of common cold or influenza

NCT ID: NCT02490566 Completed - Obesity Clinical Trials

Enhanced Primary Care and Technology for Children With Chronic Disease

Start date: July 2015
Phase: N/A
Study type: Interventional

Using technology alongside a pediatric chronic disease specialist and behavior specialist, the investigators are planning to help care for and coordinate the healthcare of children with chronic diseases, particularly childhood obesity, diabetes and asthma in Miami's most vulnerable communities. The University of (UM) Miller School of Medicine (MSOM) Pediatrics and TeleHealth departments propose to leverage information and communications technologies (ICT) in an innovative approach to improve the quality, access and efficiency of pediatric services for children and their families.

NCT ID: NCT02490358 Completed - Asthma Clinical Trials

Biomarker Assay Validation in Healthy Smokers and COPD Smokers and Ex-smokers

Start date: June 2015
Phase: N/A
Study type: Observational

This study will collect sputum samples from healthy smokers, COPD smokers and COPD ex-smokers to analyse biomarkers of inflammation