Evaluation of solid lipid nanoparticles containing Isotretinoin in treatment of acne
Phase 2
- Conditions
- Acne Vulgaris.Acne
- Registration Number
- IRCT201203283862N9
- Lead Sponsor
- ano Technology Research Center,Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Acne vulgaris patients with grade 2 and 3 base on Investigator Global Assessment; No receiving topical treatment of acne from 4 weeks before this regimen.
exclusion criteria:Androgenic acne;Acne due to drugs or cosmetics; Adrenal or Hormonal disorders.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Inflammatory and non-inflamatory lesions. Timepoint: Biweekly after starting treatment. Method of measurement: Observation and calculating of elementary lesions based on photographic image.
- Secondary Outcome Measures
Name Time Method Evaluation of side effects like skin irritation , erythema , skin dryness.pruritus. Timepoint: Biweekly. Method of measurement: Observation and severity scoring from + to +++.
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie Isotretinoin's efficacy in acne treatment via solid lipid nanoparticles?
How does solid lipid nanoparticle Isotretinoin compare to traditional retinoids in acne management?
Are there specific biomarkers that predict response to Isotretinoin-based nanoparticle therapies for acne?
What are the potential adverse events associated with solid lipid nanoparticle Isotretinoin in acne patients?
What combination therapies or alternative drug delivery systems are being explored for Isotretinoin in acne treatment?