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Clinical Trials/CTRI/2011/10/002040
CTRI/2011/10/002040
Completed
未知

TO EVALUATE THE EFFICACY OF A SKIN ANTI AGEING NUTRICOSMETIC IN WOME

Meiji India Private Ltd0 sites67 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Meiji India Private Ltd
Enrollment
67
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
December 5, 2011
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Meiji India Private Ltd

Eligibility Criteria

Inclusion Criteria

  • 1\. Women with dry skin confirmed by taking 2\. MoistureMeter SC readings (MoistureMeter SC Readings \<20\).
  • 3\. Phototype IV and below.
  • 4\. Food habit\- Non vegetarians or consented vegetarian...
  • 5\. Subjects not on any nutritional supplement or not consuming any therapeutic medication for any disorder for last 45 days.
  • 6\. Subjects with no known allergies to foods \& other substances.
  • 7\. Cooperating, informed of the need and duration of the study procedures, and ready to comply.
  • 8\. Having signed a Consent Form and will be once informed orally and in writing of all information concerning the study procedures and study objectives.

Exclusion Criteria

  • 1\.Subjects with any chronic illness or any clinical condition.
  • 2\.Subjects showing abnormal levels in blood test parameters. (Subjects having abnormal values but are Clinically fit to participate in the trial would be enrolled in the study at Principal Investigatorâ??s Discretion).
  • 3\.Pregnant Women (as confirmed via UPT) and lactating women.
  • 4\.Subjects with known allergies to food items like fish gelatine, soya, milk and milk products, egg, gluten etc and wheat flour.
  • 5\.Subjects with substance abuse (alcohol, drugs etc.)
  • 6\.Subject likely to undergo any surgery in the period of the study
  • 7\.Subjects who were on any other experimental Investigational study within last 1 month as identified during screening on visit 1 (V1\).
  • 8\.Subjects unable to comply with the protocol in the opinion of Investigators.
  • 9\.Subjects who were not to maintain regular (orderly) life.
  • 10\.Subjects having any hard damage to skin (e.g. excessive sunburn or suntan).

Outcomes

Primary Outcomes

Not specified

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