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COMPLETED
NCT07526870
NA

Intradermal Microbotulinum Toxin for Sebum Reduction and Facial Pore Improvement

Sponsor: Instituto de Oftalmología Fundación Conde de Valenciana

View on ClinicalTrials.gov

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.

Official title: Effectiveness of Intradermal Microbotulinum Toxin for the Treatment of Seborrhea and Enlarged Facial Pores: A Prospective Before-and-After Pilot Study

Key Details

Gender

All

Age Range

18 Years - 35 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2024-07-24

Completion Date

2024-11-24

Last Updated

2026-05-26

Healthy Volunteers

Yes

Interventions

DRUG

Botulinum Toxin Type A (Dysport®)

Botulinum toxin type A is administered as intradermal microinjections (microtoxin) in the periocular region using a diluted formulation. The injections are performed using a standardized technique targeting superficial dermal layers to improve skin texture and reduce fine wrinkles while minimizing muscle paralysis.

Locations (1)

✔ Instituto de Oftalmología Fundación Conde de Valenciana IAP

Mexico City, Mexico