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Radiofrequency
RF Rejuvenation for Pelvic Floor and Vagina
N/A
Waitlist Available
Led By George Kouris, MD
Research Sponsored by InMode MD Ltd.
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 3 months
Awards & highlights
No Placebo-Only Group
Summary
Evaluation of efficacy and safety of the Votiva RF system with the Forma V handpiece for vaginal treatments.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Effect of RF on Pelvic Floor Measured by Intentional Muscle Contraction Using Biofeedback EMS
Recording of Adverse Events (Safety)
Secondary study objectives
Evaluate Quality of Life Symptoms Associated With Pelvic Floor Weakness
Evaluate Quality of Life With Pelvic Floor Conditions
Evaluate Sexual Dysfunction Symptoms Associated With Pelvic Floor Weakness
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: TreatmentExperimental Treatment1 Intervention
Participants receive Votiva treatment
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Votiva
2017
N/A
~20
Find a Location
Who is running the clinical trial?
InMode MD Ltd.Lead Sponsor
24 Previous Clinical Trials
1,370 Total Patients Enrolled
George Kouris, MDPrincipal InvestigatorMidwest Plastic Surgery, 5201 S. Willow Springs Road, Suite 440 LaGrange, IL, 60525