TO CHECK THE EFFECT OF SKIN ANTI AGEING NUTRICOSMECTIC PRODUCT IN WOME

Not Applicable

Completed

• Registration Number: CTRI/2011/10/002040
• Lead Sponsor: Meiji India Private Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2011-12-05
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 67

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).

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Reduction in skin roughness and Wrinkle evaluation. <br/ ><br>2. Skin Whitening effect evaluation <br/ ><br>3. Skin elasticity <br/ ><br>4. Skin Hydration <br/ ><br>5. Self EvaluationTimepoint: At Day 0 and Week 4

Secondary Outcome Measures

Name	Time	Method
Tolerance EvaluationTimepoint: Week 4