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Allergic Asthma clinical trials

View clinical trials related to Allergic Asthma.

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NCT ID: NCT02541331 Completed - Allergic Asthma Clinical Trials

Efficacy Of Bacterial Lysate In Asthmatic Children

EOLIA
Start date: July 2014
Phase: Phase 3
Study type: Interventional

This study evaluate the efficacy of Mechanical Bacterial Lysate (PMBL - Ismigen®) to improve the asthma control level (ACT score) as add-on treatment to routine asthma treatment in children aged 6 to 16 with uncontrolled or partly controlled asthma. Half of the 150 participants will receive Ismigen® and their current asthma therapy while the other half will receive Placebo and their current asthma treatment.

NCT ID: NCT02504528 Completed - Allergic Asthma Clinical Trials

Bronchial Allergen Provocation Tests in Asthmatics in Guangzhou

Start date: July 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to establish the methodology of bronchial provocation tests with house dust mites in China, and to evaluate its safety and effects on upper and lower airways inflammation.

NCT ID: NCT02096237 Completed - Allergic Asthma Clinical Trials

Extracorporeal SPecific IgE Removal From the Plasma of Allergic Asthma Patients (ESPIRA-study)

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

In this study patients suffering from Immunoglobulin E (IgE) mediated asthma are treated with a method, called immune apheresis, that removes IgE from blood. In order to achieve this blood is taken continuously from the patient and then separated into plasma and blood cells by centrifuge. The plasma passes the new IgE adsorber where the IgE is specifically bound. The "cleaned" plasma re-joined with the blood cells is given back to the patient. In total each patient randomized to the apheresis group will undergo 3 treatments per week (i.e. 1 cycle) every 4 weeks over a time period of 3 months, that means 9 apheresis treatments in 3 cycles in total. Study hypothesis is that the new IgE adsorber is capable of reducing IgE in plasma/serum by at least 50% measured before the first treatment in the first cycle and after the last treatment in the last treatment cycle. The new adsorber can be safely used in patients. A group of patients with conventional drug treatment and no apheresis treatment serves as control.

NCT ID: NCT02023151 Completed - Allergic Asthma Clinical Trials

Predicting the Clinical Response to Omalizumab With Anti-Immunoglobulin E (IgE) Ab Response or Syk Expression in Basophils

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

This research is being done to test whether differences in blood cells at baseline (start of the study) can be used to predict how well omalizumab will work in a patient. Omalizumab (Xolair) is a drug approved by the U.S. Food and Drug Administration (FDA) to treat asthma. Studies show that omalizumab improves the symptoms of asthma but some people experience better improvement than others.

NCT ID: NCT01976208 Completed - Allergic Asthma Clinical Trials

Safety and Efficacy Study of Omalizumab to Treat Allergic Asthma

AA007
Start date: December 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The primary purpose is to evaluate the safety and efficacy of recombinant humanized anti-IgE monoclonal antibody injection in patients with allergic asthma.

NCT ID: NCT01821716 Completed - Allergic Rhinitis Clinical Trials

Biological Standardization of Dermatophagoides Pteronyssinus Allergen Extract

Start date: March 2013
Phase: Phase 2
Study type: Interventional

The objective of this study is to determine the biologic activity of a Dermatophagoides pteronyssinus allergen extract in histamine equivalent prick (HEP) units, in order to be used as in-house reference preparation (IHRP).

NCT ID: NCT01703312 Completed - Allergic Asthma Clinical Trials

A Study Evaluating the Efficacy of QGE031 Compared to Omalizumab in Patients With Allergic Asthma

Start date: November 2012
Phase: Phase 1/Phase 2
Study type: Interventional

This study will evaluate the efficacy of QGE031 compared to omalizumab in patients with allergic asthma. Each treatment's effect in changing the concentration of inhaled allergen that is required to elicit a 15% fall in the forced expiratory volume in one second (FEV1) at 12 weeks compared to baseline will be evaluated.

NCT ID: NCT01699594 Completed - Allergic Asthma Clinical Trials

Change in Airway Responsiveness After Allergen Exposure

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

Exposure to allergens changes the way the airway responds to some stimuli (methacholine). The investigators will look at whether or not exposure to allergens changes the way the airway responds to a different stimuli (mannitol) and compare that with the known stimuli (methacholine).

NCT ID: NCT01669681 Completed - Allergic Asthma Clinical Trials

Cobra (Severe Asthma)Medical-economic

Cobra
Start date: December 20, 2011
Phase: N/A
Study type: Observational

The severe asthma is a major source of expenses in term of public health, while it concerns no more than 5 % of the asthmatics. The expenses is direct (medicines, hospitalizations, care) but especially indirect (absenteeisms, etc.). The forward-looking follow-up of cohort of more than 500 severe asthmatic patients multicentrique in an already widely established cohort (COBRA, at present in Visit 9 (one every 6 months) is an once-in-a-lifetime opportunity, coupled with the data of the CPAM, to identify well the evolution in time of a real medical economic variable. The possibility of dynamic follow-up of the expenses compared to the medical data offers perspectives of evaluation cost-efficiency of the informed therapeutic procedures. It is possible to couple in a forward-looking and dynamic way the data of health stemming from a cohort with the economic data stemming from the CPAM. This variable included in a Cluster's algorithm has to allow to identify the interventions the more and the less cost effective. The main objective of this study is to realize a cost estimate of care of the severe asthma. The variation of the costs will be also studied. The recruited patients are patients already included in the cohort COBRA in the centers of Marseille, Montpelier or Nice, classified GINA 4 and agreeing to participate.

NCT ID: NCT01612715 Completed - Allergic Asthma Clinical Trials

Analysis of Fel d 1-specific T Cells After Airway Allergen Challenge in Asthma

Start date: January 29, 2014
Phase:
Study type: Observational

Cat allergies are a major trigger of asthma. Therapies are being developed to control the allergic response to cats. We are interested in measuring a type of white blood cell which is linked to cat allergies, which will help us understand how to use new therapies in people who suffer from cat allergies and asthma. We will study cat-allergic individuals with stable, mild asthma who will be exposed to cat allergens. We will measure various white blood cells, including the cells that are linked to cat allergies, to determine whether the number of these cells changes following cat exposure. These cells will be measured from the blood and bone marrow by removing samples using a needle. These cells will also be measured from the lungs by inserting a bronchoscope into the airways and drawing up fluid containing cells. This study will improve our understanding of the harmful versus protective role of these cat-specific cells, and will allow for development of better drugs for treatment of asthma triggered by cat exposure.