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Asthma clinical trials

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NCT ID: NCT01202214 Completed - Asthma Clinical Trials

Repeat Dose Safety Study for Compound to Treat Asthma

Start date: September 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to describe the safety and tolerability of single and repeat oral doses of GSK1440115 in healthy volunteers.

NCT ID: NCT01202097 Completed - Asthma Clinical Trials

A Non- Inferiority Comparative Study Between Seretide® and Salmeterol/Fluticasone Eurofarma in Patients With Asthma

CAINAS SF
Start date: August 2011
Phase: Phase 3
Study type: Interventional

The primary objective will be to compare the formulations regarding their impact on the pulmonary function of persistent asthma patients and the secondary objective will be the clinical control of the disease's symptoms.

NCT ID: NCT01202084 Completed - Asthma Clinical Trials

A Study Comparative of Formoterol/Fluticasone Foraseq® and Fluticasone in Asthma Patients

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

The primary objective will be to compare the impact of the study formulations on pulmonary function in persistent asthma carriers.

NCT ID: NCT01200446 Completed - Asthma Clinical Trials

Effect of a Component of Fish Oil on Exercise-Induced Bronchoconstriction and Airway Inflammation in Asthma

Start date: October 2010
Phase: N/A
Study type: Interventional

Docosahexaenoic acid (DHA) is a component of fish oil that is known to support a healthy cardiovascular system, maintain brain function, reduce depression, and improve inflammatory diseases. The study hypothesis is that DHA supplementation will diminish exercise-induced bronchoconstriction and airway inflammation as compared to placebo.

NCT ID: NCT01200108 Completed - Asthma Clinical Trials

AKITA Inhaled Steroid Suspension for Inhalation (AICS) in Subjects With Asthma

Start date: March 2010
Phase: Phase 2
Study type: Interventional

The goal of treatment with AICS is weaning from oral corticosteroids, i.e. a reduction of the oral corticosteroid dose. An anticipated treatment benefit of AICS is a reduction of oral corticosteroid dose and stability/improvement of clinical parameters related to asthma in the targeted subject population. Ultimately, the goal is to free subjects with severe asthma from the burden of chronic oral steroid therapy.

NCT ID: NCT01199289 Completed - Asthma Clinical Trials

A Study to Evaluate the Dosing of AMG 827 for Subjects With Inadequately Controlled Asthma

Start date: October 4, 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if AMG 827 is effective compared to placebo as measured by change in Asthma Control Questionnaire (ACQ) composite scores.

NCT ID: NCT01197690 Completed - Bronchial Asthma Clinical Trials

Association Between Fractional Exhaled Nitric Oxide and Asthma Control

FeNO_AS
Start date: February 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine mean or median of fractional exhaled nitric oxide (FeNO) in Thai atopic asthmatic patients that divided into subgroups due to level of asthma control according to the global initiative for asthma guideline.

NCT ID: NCT01197482 Terminated - Clinical trials for Severe Persistent Asthma

Inhaled Steroids and Control of Severe Asthma

INHALE
Start date: September 2010
Phase:
Study type: Observational

Investigational device: AKITA 2 device versus conventional metered-dose inhaler (MDI) Objectives: To explore if inhalative fluticasone application by means of the AKITA technology would result in a better symptom control in patients with severe persistent asthma as compared to inhalative application of fluticasone by a conventional MDI. Study design: open label, cross-over (one AKITA, one MDI arm) Patients: 20 Patients with severe persistent asthma

NCT ID: NCT01196689 Completed - Asthma Clinical Trials

Pharmacokinetics in Adolescents

PEAK
Start date: October 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to study pharmacokinetics in adolescents.

NCT ID: NCT01196377 Completed - Acute Asthma Clinical Trials

Optimal Albuterol Regimens for Acute Asthma Exacerbations: DBRCT Pilot Study

OARS
Start date: September 2010
Phase: N/A
Study type: Interventional

Our overall objective is to model a pediatric Acute Asthma Clinical Decision Rule (ADR) for personalized medicine by identification of treatment-response phenotypes that are important determinants of outcome. The Specific Aim of this study is to determine the feasibility of this approach by enrolling a pilot cohort of 16 participants in this DBRCT of 4 different albuterol treatment regimens, 2 of which will use 10mg/hr and 2 of which will use 25mg/hr. Within these dosages there will be a pulsed-treatment regimen and a continuous regimen.