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A Split-Face Comparison of Novel Microneedle Patch versus Botulinum Toxin-A and Microneedle Patch for Improvement in Undereye Skin Texture

Phase 3
Completed
Conditions
Healthy population
microneedle patch, transdermal drug delivery, wrinkle, botulinum toxin
Registration Number
TCTR20231002007
Lead Sponsor
Thammasat University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
23
Inclusion Criteria

Patients' consent was also obtained prior to the use of the images for medical purposes. Based on the Scientific Assessment Scale of Skin Quality (SASSQ) and Merz infraorbital hollow rating scale, all participants presented moderate to severe skin texture

Exclusion Criteria

there was a history of filler use within one year of study enrollment; the use of botulinum toxin injection in the previous six months; use of laser therapy in the previous six months of laser therapy; a history of light or radiofrequency use to the face; or the use of chemical peel within three months of study recruitment. Volunteers with existing infectious skin disease or eczematous dermatitis, those taking immunosuppressive therapy, women with hypersensitivity or allergy to cosmetics, those using a topical anti-wrinkle regimen for at least three months prior to recruitment, and pregnant or lactating women were also excluded from participating in the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
SASSQ skin quality rating scale 16 weeks photo
Secondary Outcome Measures
NameTimeMethod
Merz infraorbital hollow scale 16 weeks photo
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