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The Effect of Lipmatte K

U

Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre

Status

Completed

Conditions

Healthy
Cosmetic
Aesthetic

Treatments

Other: Lipmatte K

Study type

Interventional

Funder types

Industry

Identifiers

NCT05694442
UMRAMREC002-22

Details and patient eligibility

About

This study is conducted to evaluate the safety and the effectiveness of Lipmatte K on lip hydration and brightening. The study duration is 4 weeks and the lip assessment will be carried out at baseline, week 2 and week 4.The main questions this study aims to answer are:

  1. The hydration effect of the product on lip.
  2. The brightening effect of the product on lip.
  3. To observe any adverse effect occurrence with the usage of the product.

Enrollment

34 patients

Sex

Female

Ages

30 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Malaysia citizen
  • Female (age 30-55 years old)
  • Lip with mild-to-moderate dryness

Exclusion criteria

  • Subjects who have history of performing lips-related treatments such as lip augmentation (filler, botox, laser)
  • Heavy lips desquamation or chapped lip conditions

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

34 participants in 1 patient group

Lipmatte K
Experimental group
Description:
Participants will used Lipmatte K everyday for 4 weeks
Treatment:
Other: Lipmatte K

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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