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Effect of Atrovastatin on lung inflammation in bronchitis

Evaluation of the effect of Atrovastatin on inflammatory markers in sulfur mutsard gas induced chronic bronchitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138904144312N1
Enrollment
90
Registered
2014-08-16
Start date
2014-06-29
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

Chronic bronchitis. Chronic bronchitis: obstructive

Interventions

Intervention 1: Intervention group:40 mg atorvastatin daily for 3 months. Intervention 2: Control group: one placebo tablet daily for 3 months.
Treatment - Drugs
Intervention group:40 mg atorvastatin daily for 3 months
Control group: one placebo tablet daily for 3 months

Sponsors

shiraz University Of medical Science
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: exposure to mustard gas during the Iran-Iraq war and have suffered from chronic bronchitis (history of chronic cough and sputum daily for 3 months during recent 2 years) Exclusion criteria: Using statin in the last 3 months of study starting time; exacerbation of symptoms in the past 4 weeks; connective tissue disease; sarcoidosis; eosinophilic granuloma; pneumoconiosis; lymphoma; carcinomatous; smokers

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
TNF alpha level. Timepoint: before intervention - 3 month after intervention. Method of measurement: ELISA test is performed.;Interleukin 6 level. Timepoint: before intervention - 3 month after intervention. Method of measurement: ELISA test is performed.;Added at 2015-08-05: Procalcitonin. Timepoint: Added at 2015-08-05: At the beginning of the intervention and 3 months after intervention. Method of measurement: Added at 2015-08-05: ELISA.

Secondary

MeasureTime frame
Withe blood cell count. Timepoint: before intervention - 3 month after intervention. Method of measurement: Complete Blood Count.;Added at 2015-08-05: hs-CRP. Timepoint: Added at 2015-08-05: At the beginning the intervention and 3 months after intervention. Method of measurement: Added at 2015-08-05: Immunoassay.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr seyed Masoom Masoompour

Shiraz University of Medical Sciences

masoomm@sums.ac.ir+98 71 1647 4316

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 23, 2026