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Asthma clinical trials

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NCT ID: NCT01426061 Completed - Asthma Clinical Trials

Clinical Effect of Reflexology and Homeopathy Added to Conventional Asthma Management

Start date: May 2006
Phase: N/A
Study type: Interventional

There is a lack of scientific evidence that homeopathy and reflexology is effective treatment of asthma. Systematic reviews have found that many clinical trials testing homeopathy and reflexology have major flaws, such as small number of participants, lack of control groups or inadequate allocation concealment. The aim of the present study was to assess the effect of reflexology and individualised homeopathy as an adjuvant treatment in asthma. In order to address this issue, the investigators conducted an investigator-blinded, randomized, controlled parallel group study.

NCT ID: NCT01425801 Completed - Asthma Clinical Trials

Single Dose Study to Assess Efficacy, Safety and Tolerability of LAS100977 in Asthmatic Patients.

Start date: August 1, 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the pharmacodynamics of single doses of inhaled LAS100977 QD in patients with persistent asthma.

NCT ID: NCT01424813 Completed - Asthma Clinical Trials

A 12-week Study to Compare the Efficacy and Safety of Albuterol Spiromax® Versus a Placebo in People 12 Years and Older With Persistent Asthma

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

The study will measure the change in lung function in subjects with asthma after inhaling from either of two inhalers: Albuterol Spiromax® or placebo.

NCT ID: NCT01424280 Completed - Asthma Clinical Trials

Single Dose Study of GSK1440115 in Patients With Asthma

Start date: August 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess bronchodilator effect after single dose administration of GSK1440115 in a population of mild to moderate asthmatic patients.

NCT ID: NCT01424137 Completed - Asthma Clinical Trials

Inspiratory Flow Parameters of Easyhaler and Diskus Inhalers (SALIF)

SALIF
Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to characterise inspiratory flow parameters across 2 Easyhaler® (EH) inhaler versions and Diskus® inhaler in patients with asthma (including children, adults, and the elderly) and in patients with chronic obstructive pulmonary disease (COPD).

NCT ID: NCT01424124 Completed - Asthma Clinical Trials

Safety and Efficacy of YHD001 in Asthma

Start date: November 2011
Phase: Phase 2
Study type: Interventional

The main objective is to evaluate the safety/tolerability and efficacy of YHD001 compared to singulair or placebo in patients (n=96) with partially controlled asthma. The study will conduct with 4 comparative groups orally treated with YHD001 dose level 1(t.i.d.), YHD001 dose level 2(t.i.d.), singulair 10mg(q.d.) or Placebo for 8 weeks.

NCT ID: NCT01423461 Completed - Obesity Clinical Trials

Personalized Asthma Care Team

PACT
Start date: July 2005
Phase: N/A
Study type: Observational

"Individualized health care" refers to the development of strategies for disease management and health promotion that are informed by specific data on genetics and physiological processes that uniquely determine each person's health profile and potential responsiveness to interventions or susceptibility to environmental exposures. Asthma, an inflammatory disorder of the airway, appears to be determined by multiple interacting genetic and environmental factors. Such risk factors include allergic responses, small airways, excess body weight, specific properties of airway smooth muscle, airway and generalized metabolic and inflammatory homeostasis, and exposures to environmental irritants, allergens, and psychosocial stressors. To date, asthma treatment strategies have been guided by "severity" guidelines rather than by characteristics of the child's specific phenotype (a child's underlying allergic tendency, extent of airway inflammation and airway smooth muscle dysfunction, or underlying obesity and metabolic perturbations). The growing availability of new classes of asthma medications that more directly target specific pathophysiological derangements will require accessing data on each child's asthma risk profiles to optimize selection of medications and other interventions that most specifically address the underlying pathophysiology while minimizing adverse treatment side effects. The investigators propose to develop a model program for collecting relevant clinical information and genetic data on a high risk group of asthmatic children, including data on common co-morbidities, specifically obesity and sleep disorders; use this information to develop a comprehensive model database for characterizing children according to their health profiles; and use this characterization to initiate targeted interventions, while continuing long term follow up of these children to determine differential responsiveness to medications.

NCT ID: NCT01423305 Completed - Asthma Clinical Trials

Phase I Pharmacokinetic Study (BF-BLOCK)

BF-BLOCK
Start date: August 2011
Phase: Phase 1
Study type: Interventional

The objective of the study is to assess if charcoal prevents the absorption of budesonide and formoterol via GI track. The assessment will be based on comparing the pharmacokinetic parameter area under the concentration-time curve.

NCT ID: NCT01420705 Completed - Asthma Clinical Trials

Bacille Calmette-Guérin (BCG) Vaccine and Atopy

Start date: October 2011
Phase: N/A
Study type: Observational

The prevalence of asthma and allergic diseases is increasing worldwide. Infections and vaccinations in childhood may have an impact on the subsequent development of asthma and allergy. In Guinea-Bissau, the investigators previously found that Bacille Calmette-Guérin (BCG) vaccine was associated with reduction in atopy. Since then the investigators have conducted a randomised trial of BCG vaccine given at birth to low birth-weight infants. The present study aims to follow up children enrolled in the BCG randomised trial to assess for asthma and allergy later in childhood. Based on previous observations, the investigators expect children allocated to receive BCG at birth will have a reduction in allergy profile when compared to children who did not receive BCG at birth.

NCT ID: NCT01420133 Completed - Asthma Clinical Trials

Is a Diet Necessary When Corticosteroid Treatment is Prescribed?

Cortisel
Start date: November 2011
Phase: N/A
Study type: Interventional

Few recommendations concerning the diet and dosage to be administered to patients treated with corticosteroids are established. It therefore seems important to study prospectively the indication of a diet low in salt and sugar in patients undergoing corticosteroid therapy, to record side effects observed and to measure their frequency.