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Clinical Trials/TCTR20230417003
TCTR20230417003
Recruiting
Phase 4

Efficacy and Safety of using microfocused ultrasound with circular cartridge for enlarged pores in Thailand

Faculty of Medicine Siriraj Hospital, Mahidol University0 sites32 target enrollmentStarted: April 17, 2023Last updated:

Overview

Phase
Phase 4
Status
Recruiting
Enrollment
32

Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
30 Years to 50 Years (—)
Sex
All

Inclusion Criteria

  • 1\. A person with visibly enlarged pores on both cheeks that can be seen at a distance of 50 centimeters.
  • 2\. Being a Thai person of Asian descent
  • 3\. Volunteers who voluntarily agree to participate in the project

Exclusion Criteria

  • 1\. Pregnant women and breastfeeding women.
  • 2\. Had dermatitis, wounds, or skin infections on the face.
  • 3\. Subjects who had undergone thread lifting or face lifting devices or had facial surgery within 12 months of participating in the study.
  • 4\. Subjects with a history of receiving filler or botulinum toxin injections within 6 months before study participation.
  • 5\. Volunteers with uncontrolled heart disease, uncontrolled thyroid disease, autoimmune disease, taking immunosuppressant drugs, using a pacemaker, and having metal implants on the face.
  • 6\. Subjects have a history of hypertrophic scars or keloids.
  • 7\. Subjects with mental disorders whom a psychiatrist has diagnosed.
  • 8\. Subjects who are not allowed to take pictures for treatment evaluation
  • 9\. Subjects with excessive subcutaneous fat (ptotic fat)
  • 10\. Subjects taking NSAIDs, ASA, and steroids in the 72 hours before treatment

Investigators

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