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Clinical Trials/CTRI/2023/10/058750
CTRI/2023/10/058750
Recruiting
未知

A clinical study to assess moisture kinetics, brightness and anti-ageing related benefits, safety, efficacy and in-use tolerability of Day Cream, Night Cream, Skin Serum and Anti-Aging Cream - Nil

Dabur India Limited0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Dabur India Limited
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\) Age: 30 \- 55 above (both inclusive) old at the time of consent.
  • 2\) Sex: Healthy non\-pregnant/non\-lactating females.
  • 3\) Females of childbearing potential must have a self\-reported negative urine pregnancy test.
  • 4\) Subjects are generally in good general health as determined from recent medical history.
  • 5\)Subjects forearm must be free of cuts, tattoos, scratches, abrasions, scars, uneven skin tone, sunburn, excessive tan, excessive hair or open wounds on or near the test sites.
  • 6\) Subjects with mild to moderate age spots, sun spots, dark spots.
  • 7\) The subject is willing and able to follow the study directions, participate in the study, returning for all specified visits.
  • 8\) The subject must be able to understand and provide written informed consent to participate in the study.

Exclusion Criteria

  • 1\) Subject with known allergy or sensitization to product ingredients.
  • 2\) Subjects with very severe persistent spots.
  • 3\) The subject has clinically significant skin disease, which may contraindicate participation, including psoriasis, eczema, Skin cancer or other skin pathology.
  • 4\)The subject has skin irritation, open wounds, cuts, abrasions, irritation symptoms or any dermatological condition on the face that can interfere with the reading.
  • 5\)Be wearing any facial makeup, including false eyelashes, on the day of the study visit
  • 6\)Subject participation in the study involving the only one application of a personal care product such as lotion or cleansing product to the test area with no invasive procedure within the four weeks prior to enrolment.
  • 7\)Medication which may affect skin response and/or past medical history.
  • 8\)Topical drugs used at the application site.
  • 9\)An individual who has a medical condition or is taking or has taken a medication which, in the Investigator’s judgment, makes the subject ineligible or places the subject at undue risk.
  • 10\)Subjects who have been treated with systemic retinoids or steroids within the past month prior to entry to the study.

Outcomes

Primary Outcomes

Not specified

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