CTRI/2012/11/003140
Recruiting
Phase 3
A double blinded, single centered study to evaluate the efficacy of face wash, face scrub and face mask individually and when used in combination, to give salon like fresh fair look everyday on healthy female subjects.
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Hindustan Unilever Limited
- Enrollment
- 40
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Subject in generally good health.
- •2\.Subject between the ages of 18 and 30 years.
- •3\.Subject has done salon visits two times in the last one year for cleanup and facial.
- •4\.Subject with Fitzpatrick III or IV skin type.
- •5\.Subject having blackheads on face.
- •6\.Subject has not participated in a similar clinical investigation in the past four weeks
- •7\.Subject with no known allergy/ sensitivity to cosmetic products or fragrance and without any skin allergies / infections.
- •8\.Subject not under any dermatologic treatment / prescribed medications.
- •9\.Subject willing to abstain from using any cosmetic product on face, besides the provided product during the entire study course.
- •10\.Subject willing to visit the site at specified frequencies for periodic evaluations.
Exclusion Criteria
- •A known history or present condition of allergic response to any cosmetic products.
- •2\. Skin disease (e.g. psoriasis, atopic dermatitis or other cutaneous manifestations on the scalp), which would interfere with the test readings.
- •3\. Medications (e.g. steroids or antihistamines), which would compromise the study.
- •4\. Currently or has been undergoing dermatologist facial treatments or procedures within the last 1 month.
- •5\.Subject viewed by the investigator as not being able to complete the study or participating in another study.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Phase 3
To evaluate the efficacy of face wash, face scrub and face mask when used in combination, to give Clear pores effect on healthy female subjects.CTRI/2013/02/003419Hindustan Unilever Limited40
Completed
Phase 2
to evaluate the efficacy of face wash, face scrub and face mask individually and when used in combination, to give salon like Nourishing glow everyday on healthy female subjects.CTRI/2012/12/003203Hindustan Unilever Limited40
Active, not recruiting
Not Applicable
A Single-Center, Double Blind Study Evaluating the Bioequivalence of the Pharmacokinetic and Pharmacodynamic Properties of Different Formulations of VIAject™ in Subjects with Type 1 Diabetes MellitusEUCTR2008-001670-32-DEBiodel Inc.
Completed
Phase 4
The efficacy of Prontoderm® for topical decolonisation of methicillin-resistant Staphylococcus aureus (MRSA) carriersISRCTN02288276Geneva University Hospitals (Hôpitaux Universitaires de Genève) (Switzerland)160
Unknown
Phase 4
A clinical trial to study the effect of 1.5 % Aminexil and 5 % Minoxidil topical solution vs 5 % Minoxidil topical solution in male pattern hair lossHealth Condition 1: null- Male pattern of hair lossCTRI/2011/07/001856Glenmark Pharmaceuticals Ltd40