MedPath

Effect of Nigella sativa on acne vulgaris

Phase 3
Conditions
Acne Vulgaris.
Acne vulgaris
Registration Number
IRCT20180712040449N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
56
Inclusion Criteria

Patients between 14–35 years old from both genders
Patients with mild to moderate acne as defined by the Investigator’s Global Assessment (IGA) scale
Enrolled female participants should have a negative pregnancy test

Exclusion Criteria

Any aesthetic facial procedure including laser therapy and tissue/dermal injectables within the last 6 months
Patients having wound and infection on face
Patients with any skin disorders that might interfere with the diagnosis or evaluation of acne
Very severe acne vulgaris
Pregnancy or breastfeeding
Patients with any uncontrolled systemic disease
Using oral isotretinoin in the last 6 months
History of hypersensitivity to blackseed

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
People with mild to moderate acne vulgaris. Timepoint: Acne lesions counting at baseline, days 14, 30, and 60. Method of measurement: Investigator’s global assessment grading for acne vulgaris.
Secondary Outcome Measures
NameTimeMethod
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