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Effect of treatment with atorvastatin on asthma

Effect of treatment with atorvastatin on serum levels of periostin and interleukin 13 comapred with placebo in asthmatic patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017102216367N2
Enrollment
80
Registered
2017-11-15
Start date
2017-11-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma. Mixed Asthma

Interventions

Intervention 1: Intervention group: Tablets of ?Atorvastatin are product of IRAN and 40 mg. Therapy is with one tablet daily for eight weeks. Intervention 2: Control group: Placebo will be given 1 ti
Treatment - Drugs
Placebo
Intervention group: Tablets of ?Atorvastatin are product of IRAN and 40 mg. Therapy is with one tablet daily for eight weeks.
Control group: Placebo will be given 1 times daily for 8 weeks.

Sponsors

Vice chancellor for research, 7th floor, Central building of SUMS, Zand Ave
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamrad Mehrabi

Shiraz University of Medical Sciences

mehrabis@sums.ac.ir+98 71 3647 4316

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026