Health Condition 1: L700- Acne vulgaris
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Subjects of either gender 2) Subjects of 12 to 35 years of age with mild to moderate (comedones, papules and few pustules) facial acne vulgaris having more than or equal to 2 and less than equal to 30 lesions(inflammatory and/or non inflammatory) lesions
Exclusion criteria
Exclusion criteria: 1)Patients already on anti-acne medication in last one month 2) Patients having nodulocystic lesions, acne conglobata, acne fulminans, secondary acne 3) Patients unwilling to give written informed consent 4) Patients with known hypersensitivity to benzoyl peroxide, clindamycin or adapalene 5) Pregnant or lactating women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of clindamycin 1% -benzoyl peroxide 2.5% with adapalene 0.1% - benzoyl peroxide 2.5% in mild to moderate facial acne vulgaris by lesion counting.Timepoint: 4 weeks, 8 weeks and 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To compare the safety of clindamycin 1% -benzoyl peroxide 2.5% with adapalene 0.1% - benzoyl peroxide 2.5% in mild to moderate facial acne vulgaris by lesion counting by clinical examination on scale of 0 to 3. 2)To compare the cost effectiveness of clindamycin 1% -benzoyl peroxide 2.5% with adapalene 0.1% - benzoyl peroxide 2.5% in mild to moderate facial acne vulgaris by lesion counting.Timepoint: 4, 6 and 12 weeks | — |
Countries
India
Contacts
Government medical college, Nagpur