Clinical Trial

Intradermal Microbotulinum Toxin for Sebum Reduction and Facial Pore Improvement

Study acronym: MICROTOX-PORE
Completed
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Summary
This study aims to evaluate the efficacy and safety of microdoses of botulinum toxin type A (microtoxin) for improving periocular skin quality and reducing fine wrinkles. Botulinum toxin is commonly used in aesthetic medicine; however, its use in microdoses has been proposed to achieve more natural results with fewer adverse effects. Participants with periocular rhytids will receive intradermal injections of diluted botulinum toxin. Clinical outcomes will include improvement in skin texture, wrinkle reduction, and patient satisfaction. Safety will be assessed by monitoring adverse events. The findings of this study may help determine whether microtoxin is an effective and safe option for minimally invasive periocular rejuvenation.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-04-09.
Trial Details
NCT Number NCT07526870
Lead Sponsor Instituto de Oftalmología Fundación Conde de Valenciana
Conditions Facial Aging, Facial Wrinkles and Rhytides Reduction
Enrollment 30 participants
Start Date 2024-07-24
Primary Completion 2024-11-24 (estimated)
Study Completion 2024-11-24 (estimated)
Updated on ClinicalTrials.gov 2026-05-26