CTRI/2019/04/018786
Not yet recruiting
Phase 4
Comparative study of efficacy, safety and cost effectiveness of topical combination therapy with clindamycin 1% - benzoyl peroxide 2.5% versus adapalene 0.1% - benzoyl peroxide 2.5% in cases of mild to moderate facial acne vulgaris: A prospective, randomized, open label, parallel study
ConditionsHealth Condition 1: L700- Acne vulgaris
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: L700- Acne vulgaris
- Sponsor
- Government medical college Nagpur
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility 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
- •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
Outcomes
Primary Outcomes
Not specified
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