CTRI/2024/10/074954CompletedUnknown
A Consumer study to check the a sebum reduction and blemishes control activity of Asaya 10 percent Niacinamide and 1 percent Alpha Arbutin Serum
Asaya1 site in 1 country100 target enrollmentStarted: October 10, 2024Last updated:
Trial Snapshot
- Phase
- Unknown
- Status
- Completed
- Sponsor
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- Percentage change in users observed change in Sebum Reduction and Blemishes
Study Overview
Brief Summary
This is an observational, questionnaire based User test consumer study where the consumers would themselves evaluate the product efficacy after using the product for 4 weeks for its efficacy against Sebum Reduction and Blemishes Control.
Below data would be taken only at the end of the study as a subjective survey.
- reduction in Acne
2. Improvement in skin gloss
- Reduction in sebum production
Done for 4 weeks on 100 healthy volunteers
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18.00 Year(s) to 45.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Voluntary man or women between 18 and 65 years.
- •Photo type III to V.
- •Having apparently healthy skin.
- •For whom the investigator considers that the compliance will be correct.
- •Cooperating, informed of the need and duration of the examinations and ready to comply with protocol procedures.
- •Having signed a Consent Form.
- •Having valid proof of identity and age.
Exclusion Criteria
- •Pregnant or nursing mothers 2.Dermatological infection or pathology on the level of studied area 3.Hypersensitivity, allergy antecedent (to any cosmetic product, raw material or hair dye) 4.Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures 5.Chronic illness which may influence the outcome of the study 6.Subjects 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.Subject in an exclusion period or participating in another food, cosmetic or therapeutic trial.
Outcomes
Primary Outcomes
Percentage change in users observed change in Sebum Reduction and Blemishes
Time Frame: at study end only (observation after 4 weeks)
Secondary Outcomes
- Not Applicable(Not Applicable)
Investigators
Dr Robin Chugh
CCFT Laboratories
Study Sites (1)
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