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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/10/002040
Enrollment
72
Registered
2011-10-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: MEIJI COLLAGEN: COLLAGEN PEPTIDE POWDER FORMULA (MEIJI COLLAGEN) (7 g of Test Product equivalent to 5 g fish collagen). 1 sachet of Product to be taken dissolved in water taken in a con

Sponsors

Meiji India Private Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Women with dry skin confirmed by taking 2. MoistureMeter SC readings (MoistureMeter SC Readings 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

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).

Design outcomes

Primary

MeasureTime frame
1. Reduction in skin roughness and Wrinkle evaluation. 2. Skin Whitening effect evaluation 3. Skin elasticity 4. Skin Hydration 5. Self EvaluationTimepoint: At Day 0 and Week 4

Secondary

MeasureTime frame
Tolerance EvaluationTimepoint: Week 4

Countries

India

Contacts

Public ContactMr RB Mohile
rsjdr@rediffmail.com66758851

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026