Acne Vulgaris. Acne vulgaris
Conditions
Interventions
Intervention 1: Intervention group: 28 patients receive semi-solid preparations of Nigella sativa, twice daily for 60 days. Intervention 2: Control group: 28 patients receive semi-solid preparations o
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
14 Years to 35 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSamaneh Soleymani
Tehran University of Medical Sciences
Outcome results
None listed