The Effect of HFA - Beclomethasone Dipropionate Qvar on Bronchial Hyperreactivity in Preschool Children

Rambam Health Care Campus

Status and phase: Completed; Phase 2

Conditions: Asthma; Bronchial Hyperresponsiveness

Treatments: Drug: placebo; Drug: Beclomethasone dipropionate HFA

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT01006655

qvar-adenosineCTIL

Details and patient eligibility

About

Respiratory diseases including Asthma are high prevalent among preschool children. Specific treatment, nowadays, include steroid inhalers and anti leukotrienes. It is known that the amount of the drug reaching small airways and lungs is bigger how much smaller the particles liberated by inhalers. Beclometasone is being used for treating asthma for 30 years. Lately emerged a new presentation of beclometasone, which liberates particles as small as 2.1 µg, that is supposed to reach the small airways at higher concentrations and be more suitable to patients who don't cooperate properly to the procedure of inhalation.

The investigators' group has reported successfully the possibility to perform Pulmonary Challenge tests (adenosine, methacholine and exercise) in tender age. Other studies reported relation between asthma control and reduction in airway hyperreactivity. The purpose of this study is to evaluate the efficacy of Beclometasone dipropionate - Qvar to reduce airways hyperreactivity in preschool children, as demonstrated by adenosine challenge test.

Full description

26 - 30 patients, between 3 -6 years old, mild asthmatics, with positive adenosine challenge test, will received in a randomized, double blind, cross over assignment Beclometasone dipropionate (100µg twice a day) or placebo, through an inhaler (autohaler) device, attached to a spacer device, during four consecutive weeks. Adenosine Challenge test will be performed another time at the end of this four weeks period. After 2 weeks with no medication (wash out period) the patients will receive the second intervention (beclometasone dipropionate or placebo) in a cross over manner and will be submitted to the last adenosine challenge test.

Clinical evaluation, resting spirometry and subjective evaluation through an analogical symptoms scale will be recorded in each visit.

Enrollment: 21 patients

Sex: All

Ages: 3 to 7 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• clinical diagnosis of mild asthma
• children aged between 3 - 6 years old
• able to perform spirometry and adenosine challenge test
• positive challenge test at the time of inclusion
• without prophylactic treatment for asthma
• signed informed consent to join the research by the parents or legal tutor

Exclusion criteria

• other chronic diseases
• use of oral steroids in the last two months
• emergency room visit in the last two months
• pneumonia in the last two months
• impossibility to perform lung function tests
• disagreement of the parents or legal tutor

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Triple Blind

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21 participants in 2 patient groups, including a placebo group

placebo, adenosine challenge test

Placebo Comparator group

Description:

Controlled or partially controlled multiple trigger wheezing children received 4 weeks of placebo, preceded and succeeded by AMP challenge test,

Treatment:

Drug: placebo

Qvar, adenosine challenge test

Active Comparator group

Description:

Patients will receive 4 weeks of inhale QVAR (HFA beclomethasone) 100µg through a spacer device, twice a day

Treatment:

Drug: Beclomethasone dipropionate HFA