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The Effectiveness of a Novel Lip Product Containing Caulerpa Lentillifera Extract for Reducing Lip Hyperpigmentation

The Effectiveness of a Novel Lip Product Containing Caulerpa Lentillifera Extract for Reducing Lip Hyperpigmentation

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07067879
Enrollment
30
Registered
2025-07-16
Start date
2025-07-23
Completion date
2025-08-13
Last updated
2025-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperpigmentation

Keywords

Lip hyperpigmentation, Seaweed, Antera3D, Lip care

Brief summary

The goal of this clinical trial is to evaluate the efficacy of the novel lip product containing Caulerpa lentillifera extract on the appearance and perception of dark lips in Thai adults aged 18 to 60 who report concerns about darkened lips. The main question it aims to answer is: Can the novel lip product containing C. lentillifera extract will significantly improve the appearance and perception of dark lips in Thai adults by reducing hyperpigmentation compared to baseline measurements? Participants will apply the lip product twice a day, in the morning after breakfast and before bedtime, and refrain from using other lip products throughout the clinical trial period (7 days). Researchers will compare the result to baseline measurements

Interventions

OTHERLip product

Lip product containing Caulerpa lentillifera extract

Sponsors

Chulalongkorn University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Understand the study protocol and provide informed consent after being informed of potential risks and benefits. * Refrain from using any other lip products, including lipstick, lip gloss, or lip conditioners, during the study period.

Exclusion criteria

* Have a known allergy or sensitivity to cosmetic products or Caulerpa lentillifera. * Are on medication one month prior to study commencement. * Exhibit lip abnormalities such as malformation, inflammation, swelling, or sores.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in improving lip hyperpigmentationBaseline and 7 daysLip hyperpigmentation is assessed using Antera3D at baseline and 7 day after usage

Secondary

MeasureTime frameDescription
Change from baseline in improving lip drynessBaseline and 7 daysLip dryness is assessed using Fotofinder system at baseline and 7 day after usage
Subjective assessment by participantsBaseline, day 1, and day 7Participants' evaluations will be collected through an online self-reported questionnaire. Subjective perceptions of lip color and dryness will be assessed using a 0-10 numerical darkness and dryness scale. Additionally, a satisfaction rating questionnaire will be administered to assess participant satisfaction with their lip appearance and the lip product on day 1 and day 7. The questionnaire will evaluate six key aspects of product performance; 1. Overall satisfaction 2. Effectiveness in hydration and moisturization 3. Improvement in lip color and texture 4. Ease of use and packaging design 5. Sensory attributes such as texture and scent 6. Occurrence of any adverse reactions

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026