Effect of Simvastatin gel in treatment of acne
Phase 2
Recruiting
- Conditions
- Acne Vulgaris.Acne vulgaris
- Registration Number
- IRCT20100119003106N38
- Lead Sponsor
- Islamic Azad University, Pharmaceutical Sciences Branch
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Patients with mild and moderate acne vulgaris
Exclusion Criteria
Pregnant women
Breastfeeding women
The patients with dermatological malignancy
The patients with burning
The patients with infection
The patients which have known hypersensitivity to simvastatin
The patients which have received any topical or oral medications for acne vulgaris in the last one month
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acne scores in the Global Acne Grading System. Timepoint: Before intervention and 2, 5 , 8 weeks after intervention. Method of measurement: The Global Acne Grading System Formula.
- Secondary Outcome Measures
Name Time Method Quality of life score. Timepoint: Before intervention and 2, 5, 8 weeks after intervention. Method of measurement: The Cardiff Acne Disability Index questionnaire.