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Clinical Trials/CTRI/2019/03/018233
CTRI/2019/03/018233
Completed
N/A

Clinical study to evaluate the effectiveness of a test face gel for moisturizing and enhancing skin health.

Ramaiah Indic SPecialty Ayurveda0 sites50 target enrollmentTBD
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Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Ramaiah Indic SPecialty Ayurveda
Enrollment
50
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
June 8, 2019
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Ramaiah Indic SPecialty Ayurveda

Eligibility Criteria

Inclusion Criteria

  • •1\.Male and female healthy volunteers, with age 18â??45 years
  • •2\.Subjects willing and able to provide informed consent voluntarily
  • •3\. Subjects having normal to moderate dry skin as assessed on the 4\-point scale given below
  • •4\.Willing to maintain the investigational product use throughout the study.
  • •5\.Subjects who have not undergone any skin therapy (eg. De\-tan, etc.) in last 3 months
  • •6\.Subjects with no known allergy to any of the test ingredients
  • •7\.Subjects who are willing to refrain from using any skin care product for the face other than the investigational product, like, moisturizers, lotions and face creams, for the duration of the study
  • •8\.Subjects willing and able to comply with all trial requirements.
  • •9\.Laboratory workup within normal limits; including complete hemogram, glucose, blood urea nitrogen, creatinine, liver function test, lipid profile, thyroid\-stimulating hormone, urine pregnancy test

Exclusion Criteria

  • •1\.Subjects who have skin diseases like psoriasis, atopic dermatitis , severe dry, self\-approved acne etc. at the time of screening
  • •2\. Subject with chronic systemic illnesses or treatment that can affect skin health eg. Dialysis
  • •3\.Subjects on oral medications or suffering from chronic illness which will compromise the study
  • •4\.Subjects who have participated in a similar investigation in the past four weeks
  • •5\.Pregnant or lactating women

Outcomes

Primary Outcomes

Not specified

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