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Clinical Trials/CTRI/2012/12/003189
CTRI/2012/12/003189
Completed
未知

Efficacy evaluation of Menâ??s Under Eye Serum on healthy human male volunteers.

ITC RD CENTRE0 sites35 target enrollmentTBD
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
ITC RD CENTRE
Enrollment
35
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
ITC RD CENTRE

Eligibility Criteria

Inclusion Criteria

  • •1\.Male subjects in generally good health.
  • •2\.Subjects in the age group of 25 to 65 years.
  • •3\.17\-18 subjects with moderate to severe under eye dark circles, 17\-18 Subjects with
  • •puffiness, 17\-18 Subjects with moderate to severe fine lines and wrinkles in addition to
  • •either of the above mentioned conditions.
  • •4\.Subjects free of any obvious infection of skin as determined by dermatologist.
  • •5\.Subject has not participated in a similar investigation in the past four weeks.
  • •6\.Subjects have not used a similar product for the last four weeks.
  • •7\.Subjects willing to give a written informed consent and come for regular follow up.

Exclusion Criteria

  • •1\.Subjects with known allergies or sensitivities to cosmetic products, toiletries or its components like fragrances, preservatives, hydroquinone, vitamin C, Niacin amide, retinol, soy etc.
  • •2\.Currently or has been using a similar type of product within the last 1 month.
  • •3\.Currently or has been undergoing dermatologist skin treatments or procedures within the last 1 month.
  • •4\.Currently or has been involved in another skin care clinical investigation within the last 1 months.
  • •5\.Subjects who have pre\-existing or dormant dermatologic conditions (e.g., psoriasis, rosacea, rashes, eczema, many and/or severe excoriations etc.) that could interfere with the outcome of the study as determined by the investigator.
  • •6\.Subjects viewed by the investigator as not being able to complete the study.

Outcomes

Primary Outcomes

Not specified

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