Effects of Microtox on Facial Skin Quality, Fine Wrinkles, and Texture

Description

The goal of this split-face clinical trial is to test the efficacy of microtox in improving facial skin quality, fine wrinkles, and texture. Participants will: * be randomly assigned to Group A (which will receive 20 units of neuromodulator on the left side of the forehead and a placebo saline treatment on the right side) or Group B (which will receive 20 units of neuromodulator on the left side of the forehead and 20 units of a different neuromodulator brand on the right side as a comparator) * have one treatment session at week 0, and two live assessment visits at weeks 2 and 12 * have their pictures taken at each visit to track progress

Conditions

Skin Aging, Skin Wrinkling

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Study Overview

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Study Details

Study overview

The goal of this split-face clinical trial is to test the efficacy of microtox in improving facial skin quality, fine wrinkles, and texture. Participants will: * be randomly assigned to Group A (which will receive 20 units of neuromodulator on the left side of the forehead and a placebo saline treatment on the right side) or Group B (which will receive 20 units of neuromodulator on the left side of the forehead and 20 units of a different neuromodulator brand on the right side as a comparator) * have one treatment session at week 0, and two live assessment visits at weeks 2 and 12 * have their pictures taken at each visit to track progress

Effects of PrabotulinumtoxinA-xvfs on Facial Skin Quality, Fine Wrinkles, and Texture

Effects of Microtox on Facial Skin Quality, Fine Wrinkles, and Texture

Condition
Skin Aging
Intervention / Treatment

-

Contacts and Locations

Pasadena

K. Kay Durairaj, MD, A Medical Corp., Pasadena, California, United States, 91105

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Biological females, 18-65 years old, of any race and ethnic background
  • * Individuals with mild to moderate facial wrinkles
  • * All skin types (Fitzpatrick I-VI)
  • * Willingness to participate and provide written informed consent
  • * Ability to follow study instructions and likely to complete all required visits
  • * Females who are pregnant, breastfeeding, chronically using nonsteroidal anti-inflammatory drugs, have autoimmune conditions or have a known allergy to the study medications.
  • * Previous cosmetic procedures near the forehead within the last 6 months or botulinum toxin treatments within the last 4 months
  • * Known neuromuscular disorders or a hypersensitivity to botulinum toxin
  • * Significant dermatological conditions affecting the face
  • * Use of medications affecting neuromuscular function or skin healing within 2 weeks prior to the beginning of study
  • * Subject has a condition or is in a situation which, in the opinion of the Investigator, may put the subject at significant risk, may confound the study results, or may interfere significantly with participation in the study.

Ages Eligible for Study

18 Years to 65 Years

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Kalpna Kay Durairaj, MD, FACS,

Kalpna K Durairaj, MD, PRINCIPAL_INVESTIGATOR, K. Kay Durairaj, MD, A Medical Corp.

Study Record Dates

2025-02