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Effect of treatment with atorvastatin on asthma

Phase 3
Recruiting
Conditions
Asthma.
Mixed Asthma
Registration Number
IRCT2017102216367N2
Lead Sponsor
Vice chancellor for research, 7th floor, Central building of SUMS, Zand Ave
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

Asthma patients with a history of more than one year, aged 18 till 60 years are enrolled. Exclusion criteria: Lower respiratory infection 4 weeks before entering the study; more than 10 pack-year of smoking or smoking in the last 3 months; pregnancy or breastfeeding; current use of statins or previous side effects of statin or drugs that interact with statins such as antifungal, antibiotic macrolide, cyclosporine, germifibrosil, verapamil and amiodarone; hepatitis or active liver disease; myopathy or myositis.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum level of periostin. Timepoint: Befor intervention and eight weeks after intervention. Method of measurement: ng/mL.;Serum level of IL-13. Timepoint: Befor intervention and eight weeks after intervention. Method of measurement: pg/mL.
Secondary Outcome Measures
NameTimeMethod
Adverse drug/placebo reaction. Timepoint: 4 and 8 weeks after intervention. Method of measurement: Ask from the patient and laboratory data.;Forced expiratory volume in first second. Timepoint: Before intervention and 4 and 8 weeks later. Method of measurement: liters per minute.
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