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Effect of atorvastatin in plaque-type psoriasis

Efficacy of atorvastatin in patients with plaque-type psoriasis: a randomized, double-blind, placebo-controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138807111764N2
Enrollment
60
Registered
2009-11-01
Start date
2009-03-02
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

psoriasis. Psoriasis vulgaris

Interventions

Intervention 1: Intervention: Atorvastatin Tablet 40 mg, one tablet /day. Intervention 2: Placebo tablet, one tablet per day.
Treatment - Drugs
Placebo
Intervention: Atorvastatin Tablet 40 mg, one tablet /day
Placebo tablet, one tablet per day

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1- Diagnosis of acute or chronic plaque-type psoriasis. 2- Patients with moderate disease severity (BSA involvement of at least 10% and PASI score between 12-21%). 3- Male or female patients with age range of 16-60 years. 4- Patients who have not been treated with atorvastatin or other statins within one month prior to study participation. Exclusion criteria: 1- Patients with types of psoriasis other than plaque. 2- Patients who are candidate to receive atorvastatin or other statins due to other medical conditions at trial entry and any time during the trial. 3- Pregnancy 4- Lactation 5- Having contraindications to atorvastatin. 6- Patients' refusal to participate. 7- Patients who are candidate to receive systemic therapy or phototherapy for psoriasis at the time of study entry or any time during the study. 8- Patients who are candidate to receive topical therapies other than allowed at the time of study entry or any time during the study. 9- Patients with psoriatic arthritis. 10- Systemic therapy and phototherapy for psoriasis within 30 days prior to study participation. 11- Topical therapy for psoriasis (other than allowed) within 2 weeks of study participation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Psoriasis disease severity. Timepoint: Baseline, every 4 weeks, end of week 12. Method of measurement: PASI score (standard methods).;Body surface area (BSA). Timepoint: Baseline, every 4 weeks, end of week 12. Method of measurement: Standard method.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. T. Faghihi

Tehran University of Medical Sciences

tfaghihi@razi.tums.ac.ir+98 21 6695 4709

Outcome results

None listed

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