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

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)

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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)