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Focused Ultrasound
calcium hydroxylapatite (Radiesse) and IFUS (Ulthera) for Loose Skin
Phase 1
Waitlist Available
Led By Natasha Mesinkovska, MD, PhD
Research Sponsored by University of California, Irvine
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 weeks
Awards & highlights
Study Summary
This trial found that a combination of focused ultrasound and calcium hydroxylapatite was more effective than either treatment alone for skin laxity and volume restoration in the lower thighs.
Eligible Conditions
- Loose Skin
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Efficacy of combined therapy at 12 weeks
Secondary outcome measures
Efficacy of combined therapy at 24 weeks
Efficacy with Merz Aesthetic scale at 12 and 24 weeks
Patient satisfaction at 24 weeks
Trial Design
1Treatment groups
Experimental Treatment
Group I: Combined microfocused ultrasound and calcium hydroxylapatiteExperimental Treatment1 Intervention
One-time intense microfocused ultrasound with calcium hydroxylapatite injection to one anterior lower thigh with option for additional filler injection at 6 weeks, 12 weeks, and 24 weeks. Optional combined treatment of the opposite lower anterior thigh at week 24 with no further follow up.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Calcium
Not yet FDA approved
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
University of California, IrvineLead Sponsor
543 Previous Clinical Trials
1,922,981 Total Patients Enrolled
Natasha Mesinkovska, MD, PhDPrincipal InvestigatorUniversity of California, Irvine
1 Previous Clinical Trials
200 Total Patients Enrolled
Frequently Asked Questions
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