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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