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Effect of topical Cedar on Acne

Phase 3
Recruiting
Conditions
Acne vulgaris.
Acne vulgaris
Registration Number
IRCT20171112037409N1
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
110
Inclusion Criteria

Subjects in age of 15 to 45 years old
Chief complaint: mild to moderate Acne vulgaris
subject willingness of herbal topical medicines use

Exclusion Criteria

pregnancy
lactation
History of polycyctic ovary
use of acnegenic medications such as corticosteroid, hurmonal or anti-psychotic medications
mechanical acne and gram-negative folliculitis
History of dermal allergy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total lesion count. Timepoint: at the beginning of the study, 2nd, 6th and 8th weeks. Method of measurement: counting the comedones, papules and pustules.;Severity of Acne. Timepoint: at the beginning of the study, 2nd, 6th and 8th weeks. Method of measurement: Acne Severity Index.
Secondary Outcome Measures
NameTimeMethod
Adverse effects including redness, burning and itching. Timepoint: 2nd, 6th and 8th weeks of study. Method of measurement: observation and physical examination.
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