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Therapeutic efficacy of atorvastatin in chronic idiopathic utricaria

Therapeutic efficacy of atorvastatin in chronic idiopathic utricaria

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110033862N8
Enrollment
66
Registered
2011-10-17
Start date
2010-10-21
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

Idiopathic urticaria. Idiopathic urticaria

Interventions

Intervention 1: one tablet Atorvastatin (40mg/Kg) every 12 hours (twice daily) in patient group until 3 month. Intervention 2: one tablet placebo every 12 hours (twice daily) until 3month in control g
Treatment - Drugs
Placebo
one tablet Atorvastatin (40mg/Kg) every 12 hours (twice daily) in patient group until 3 month.
one tablet placebo every 12 hours (twice daily) until 3month in control group

Sponsors

Research Council of Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: presence of utricaria more than 8 weeks, Normality of thyroids assay test, Negativity of antithyroglobulin, antimicrosomal antibodies and skin prick test for inhale and oral common allergens Exclusion criteria: Addiction, Systemic and chronic diseases, Pregnancy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Utricaria severity. Timepoint: Baseline and at the end of treatment course. Method of measurement: Utricaria severity is calculated according to Breneman et al to 4 categories; Mild, Moderate and sever.

Secondary

MeasureTime frame
Cytokines Variations. Timepoint: baseline and after the treatment course. Method of measurement: Measuring selective cytokines by Eliza method in lymphocyte culture.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Farahzad Jabbari

Allergy Research Center, Mashahd University of Medical Sciences

arc@mums.ac.ir+98 51 1843 6626

Outcome results

None listed

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