ConditionSkin Texture
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe University of Texas Health Science Center, Houston
About this trial
The purpose of this study is to evaluate whether microneedling RF subcutaneous fat pad thickness in the temple, submental, and cheek regions, to determine whether the addition of topical PLLA after microneedling RF alters or preserves subcutaneous fat pad thickness and to assess patient satisfaction and perceived outcomes following microneedling RF ± PLLA treatment.
Eligibility criteria
Qualifiers
Seeking facial rejuvenation for cosmetic concerns
Able and willing to provide informed consent
Willing to comply with study procedures and follow-up visits
Disqualifiers
Prior filler injection or energy-based device treatment to the face within the past 6 months
Previous facial surgeries
Pregnant or breastfeeding
Active infection, dermatitis, or open lesions in the treatment area
Trial design
Treatments tested in this trial
- microneedling RF treatment
- PLLA
- Sterile Water as control
Treatment groups
30 Participants
are divided into 4 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov