Evaluating the effect of topical N-acetyl cysteine in treatment of acne
Phase 3
Recruiting
- Conditions
- Acne.Acne vulgarisL70.0
- Registration Number
- IRCT20230921059485N1
- 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 moderate Acne
married females who agree with taking oral contraceptive pills (OCP) during treatment
Exclusion Criteria
below 15 or over 35 years old
unwillingness to participate in the study
inability to come regularly for follow-up visits
use of herbal medicine
receiving systemic anti acne therapies 1 month before the study
receiving topical anti acne therapies 2 weeks before the study
pregnancy and breast feeding
hepatic diseases
renal diseases
use of nitroglycerine
use of medications that have interaction with the drugs used in the study
history of hypersensitivity to the medications used in the study
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method