To study the reduction in pimples.
- Registration Number
- CTRI/2022/06/043346
- Lead Sponsor
- CLAIMS PVTLTD
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 12
1. Voluntary men/women with mild to moderate inflammatory acne between 18 years 40 years.
2. No treatment for acne in the past 1 month
3. Accepting not to use products with the same end benefit during the entire study duration.
4. For whom the Investigator considers that the compliance will be correct.
5. Cooperating, informed of the need and duration of the examinations, and ready to comply with protocol procedures.
6. Having signed a Consent Form and will be once informed orally and in writing of all information concerning the study procedures and study objectives.
1. Pregnant women (by UPT) and lactating women.
2. History suggestive of any hormonal problems.
3. History of allergic dermatitis or contact allergy to cosmetics,
4. Hypersensitivity to any cosmetic product,
5. Any clinically significant systemic or cutaneous disease, which may interfere with study treatments or procedures.
6. Participants on any medical treatment either systemic or topical which may interfere with the performance of the study treatment (presently or in the past 1 month).
7. Participant in an exclusion period or participating in another similar cosmetic or therapeutic trial.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate reduction in acne post treatment in 2 groups given different treatments from baseline. <br/ ><br>Timepoint: Day 0, Day 15
- Secondary Outcome Measures
Name Time Method To compare of the reduction in acne post treatment in 2 groups given different treatments. <br/ ><br>Timepoint: Day 0, Day 15