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Clinical Trials/CTRI/2012/11/003140
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.

Hindustan Unilever Limited0 sites40 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

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

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