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Clinical Trials/CTRI/2021/09/036560
CTRI/2021/09/036560
Completed
Phase 4

A Clinical Study to assess the safety and efficacy of kanaka taila for its anti wrinkle and skin brightening effect in healthy volunteers - KT2021

Ms Ozone Pharmaceuticals Ltd0 sites50 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Ms Ozone Pharmaceuticals Ltd
Enrollment
50
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
April 20, 2022
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
Ms Ozone Pharmaceuticals Ltd

Eligibility Criteria

Inclusion Criteria

  • Volunteers meeting the following criteria will be enrolled:
  • ïâ??· Between the age of 18\-65 years;
  • ïâ??· Available for 3 study visits;
  • ïâ??· Fine lines/wrinkles: Allergen fine lines (ââ?°Â¥ grade 1\)
  • ïâ??· Individuals who are willing to provide written informed consent
  • ïâ??· Individuals willing not to wear makeup or use skin care products other
  • than the study products the day of the study visits;
  • ïâ??· Individuals willing to discontinue using current skincare products and
  • only use study products for the study duration.
  • ïâ??· Individuals willing to refrain from sun tanning / sun bathing for the study

Exclusion Criteria

  • Volunteers will be excluded from the study if they meet any of the criteria listed
  • ïâ??· Any medically diagnosed chronic skin problems on their face (e.g.,
  • psoriasis, eczema, seborrheic dermatitis, or chronic cystic acne, etc.)
  • ïâ??· Diagnosed with known allergies to facial skin care products
  • ïâ??· Have undergone dermatological skin rejuvenation procedures such as
  • light\-therapies (lasers, radiofrequency and other lights treatments ) or
  • such as collagen or other facial tissue augmentation, fillers, or retail
  • micro dermabrasion on the face within the last 1 year preceding the
  • baseline visit and intended to receive them during the study period
  • ïâ??· Have planned surgeries or invasive procedures during the course of the

Outcomes

Primary Outcomes

Not specified

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