Cheilitis
Conditions
Keywords
Cheilitis, Aging, Lip roughness, Prevention
Brief summary
* The goal of this clinical trial is to evaluate the efficacy of the novel polyherbal lip hydrant on dryness, fine lines and color of the lips in 66Thai people aged between 18-40 years old. The inclusion criteria will include subjects with subjective complaint of dry lips.The main question it aims to answer is Does the novel polyherbal lip hydrant improve biophysical barrier of the lips? * Participant will be asked to apply the lip hydrant or the petroleum gel once a day before bedtime, and refrain from using other lip products throughout the clinical trial period (28 days). * Researchers will compare control group (Petroleum gel) with lip hydrant group to see whether biophysical barrier (wrinkles, colors, fine lines, roughness) improve or not.
Interventions
OTHERLip hydrant
lip hydrant containing peppermint oil, perilla frutescens, and Emblica fruit extract or petroleum gel.
OTHERPetroleum gel
Vaseline
Sponsors
Chulalongkorn University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)
Intervention model description
This randomized, double-blind, controlled trial will be conducted at the Faculty of Dentistry, Chulalongkorn University. The 66 participants will be randomly assigned to receive either lip hydrant containing peppermint oil, perilla frutescens, and Emblica fruit extract or petroleum gel. Both lip products will be given to allocated participants in the product container of identical appearance. Both subjects and investigators will be blinded to the study randomization.
Eligibility
Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes
Inclusion criteria
* subjects with subjective complaint of dry lips; * agree to comply with the study protocol * agree not to apply any other products such as lipstick, lip gloss, lip conditioner to the lips other than the test product for the duration of the study * provide a written informed consent prior to study enrollment.
Exclusion criteria
* Participants those having visible skin conditions which might interfere with the outcome assessment * having a history of sensitivities to cosmetics products, or moisturizers; - having a known or suspected intolerance or hypersensitivity to herbal products or any of its ingredient * taking medication or under the care of a doctor for one month prior to the commencement of the study, and throughout the entire test period * having other types of cheilitis except cheilitis simplex.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Objective evaluation | 30 minutes per 1 participant | Objective evaluation; using * Fotofinder to take a photograph of the lips. * Modified visual assessment scale to assess lip roughness score divided to 4 levels (1=not dry 2= dry without desquamated 3 = dry with slightly desquamated 4 = dry with heavy desquamated) and lip wrinkle score divided into 3 levels (1 = Almost no vertical wrinkle 2 = No deep vertical wrinkle 3= Many deep vertical wrinkle) * Antera 3D. (Texture, wrinkle, melanin pigment and hemoglobin) the value from Antera appear as the number with no unit, * Digital camera to evaluate overall clinical improvement of the lips |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Subjective evaluation | 5 minutes per 1 participant | will be assessed at day 0 (baseline), day 1 and day 28 by using a self-reported questionnaire in scale from 1-10 points for patient's dry lip score which higher score means more dry lip feeling |
Countries
Thailand
Outcome results
None listed