Effect of Hypochlorite Sodium 0.005% in treatment of Acne
Phase 2
Recruiting
- Conditions
- Acne Vulgaris.Acne vulgarisL70.0
- Registration Number
- IRCT20200701047976N1
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Patients with mild to moderate Acne Vulgaris diagnosed by dermatologist
Exclusion Criteria
Patients with symptoms such as secondary Acne caused by lactation
Dermatology condition in addition to Acne
Patients who had taken drugs such as Isotretinoin or systemic/topical antibiotics within the last two months
Allergy to Hypochlorite Sodium
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of Acne remission on the basis of changes in the number of Papules and Pustules. Timepoint: Initiation of study(before starting the treatment), 14 days and 28 days after starting the treatment. Method of measurement: Counting the number of Papules and Pustules.
- Secondary Outcome Measures
Name Time Method