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Clinical Study to Evaluate the Impact of aKwa Skincare System on Skin Health

4

4Life Research

Status

Completed

Conditions

Skin Wrinkles
Facial Skin Red Spots
Skin Hydration
Facial Skin Red Vasculature
Sin Health
Skin Porphyrins

Treatments

Other: äKwä skincare system products
Other: competitor products (control)

Study type

Interventional

Funder types

Industry

Identifiers

NCT05476406
RSC-017-00

Details and patient eligibility

About

The purpose of the study was to evaluate the effectiveness of the äKwä 6-step skincare system by measuring skin moisture level, fine lines and wrinkles, porphyrin count, red spots, and red vasculature counts over a 30-day period.

Full description

The äKwä 6-step skincare system is comprised of various skincare products intended to be applied both morning and night. Some of the notable ingredients included in the product formulas are fermented green tea water, other ferments, niacinamide, antioxidants, and a variety of natural plant extracts. The purpose of the study was to evaluate the effectiveness of the äKwä 6-step skincare system by measuring skin moisture level, fine lines and wrinkles, porphyrin count, red spots, and red vasculature counts over a 30-day period.

Enrollment

26 patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Individuals could participate who were at least 18 years old and in good health.

Exclusion criteria

  • had allergies or contraindications to any ingredient of products,
  • had a history of any acute or chronic disease that could interfere with or increase the risk of study participation
  • had any medical procedures, such as laser resurfacing, or plastic surgery to the test sites within the last 12 months (including Botox, Restylyn, or other fillers)
  • chronic skin allergies (dermatitis, eczema, psoriasis)
  • had been treated for skin cancer within the last 12 months or have damaged skin near the facial area (e.g., sunburn, tattoos, scars, or other disfigurations)
  • pregnant or planning to become pregnant in the following 12 weeks, or lactating

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

26 participants in 2 patient groups

äKwä Group
Experimental group
Description:
participants use äKwä products daily as instructed for 30 days
Treatment:
Other: äKwä skincare system products
Control Group
Active Comparator group
Description:
participants use a competitor products daily as instructed for 30 days
Treatment:
Other: competitor products (control)

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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