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Multi-polar RF and PEMF for Treatment of Vulvovaginal Atrophy

Primary Purpose

Genitourinary Syndrome of Menopause, Vulvovaginal Atrophy, Menopause

Status

Completed

Phase

Not Applicable

Locations

Ukraine

Study Type

Interventional

Intervention

Radiofrequency and pulsed electro-magnetic fields treatment

About this trial

This is an interventional treatment trial for Genitourinary Syndrome of Menopause focused on measuring Genitourinary Syndrome of Menopause, Menopause, Multi-polar Radio Frequency, Pulsed Electromagnetic Field, Sexual Dysfunction, Vaginal Laxity

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

Healthy female subjects, ≥19 years of age presenting with symptoms associated with GSM/VVA.
Requesting treatment for vulvovaginal tissue for improvement of symptoms associated with GSM/VVA, with a score of ˂26.55 on the FSFI.
Sexual activity (vaginal intercourse minimum twice per month) in a monogamous relationship.
At least one full-term pregnancy (>36 weeks gestation) with vaginal delivery completed at least one year before study enrollment.

Exclusion Criteria:

Pregnant or intending to become pregnant during the course of study.
Having any active electrical implant anywhere in the body, such as a pacemaker or an internal defibrillator.
Having a permanent implant in the treated area (e.g. intrauterine device)
Prior use of collagen, fat injections and/or other methods of skin augmentation (enhancement with injected or implanted material) in the treated area within 4-6 weeks of the initial treatment or during the course of the study.
Use of retinoids such as oral Isotretinoin (Accutane®) within 6 months of initial treatment or during the course of the study.
Any other surgery in treated area within 12 months of initial treatment or during the course of the study.
Open laceration, abrasion, bleeding, infection or inflammation of any sort on or in the area to be treated.
Active sexual transmitted disease (STD) (e.g. genital Herpes Simplex, condylomata) or vaginosis.
Chronic vulvar pain or vulvar dystrophy.
History of immunosuppression/immune deficiency disorders (including HIV infection or AIDS) or use of immunosuppressive medications, including corticosteroids, 6 months prior to and during the course of the study.
Having any form of active cancer at the time of enrollment and during the course of the study.
Significant concurrent illness, such as uncontrolled diabetes i.e. any disease state that in the opinion of the Investigator would interfere with the treatment, or healing process.
Participation in a study of another device or drug within 1 month prior to study enrollment or during this study, and as per the Investigator's careful discretion, as long as not contradictory to any of the above criteria.
Mentally incompetent or evidence of active substance or alcohol abuse.
Having any stage 3-4 cystocele, rectocele, enterocele paravaginal defect or major pelvic organ prolapse beyond the hymenal ring.
Unstable dosages of medications such as antihypertensives or psychotropics that are known to affect sexuality.
Skin piercing in the treatment area.
Tattoos in the treatment area.
Prior skin treatment with laser in the treated area within 6 months of the initial treatment or during the course of treatment.
Prior ablative resurfacing procedure in the treated area with laser or other devices within 12 months of the initial treatment or during the course of treatment.
History of keloid formation or poor wound healing in a previously-injured skin area.
History of epidermal or dermal disorders (particularly if involving collagen or microvascularity).
Menstruation less than 7 days prior to treatment.

Sites / Locations

Cogerent Laser Clinics Group

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Vulvovaginal treatment

Arm Description

Internal vaginal treatment monthly for 3 treatments.

Outcomes

Primary Outcome Measures

Vaginal Health Index

Clinician assessed improvement in five vaginal parameters; (1) vaginal fluid volume, (2) moisture, (3) vaginal epithelial integrity, (4) elasticity and (5) vaginal pH. Assessed by the clinician at each visit with baseline comparison made at the one-month and four-month post-treatment assessments.

Clinician assessed improvement (reduction) in vaginal pH with baseline comparison made at the one-month and four-month post-treatment assessments.

Secondary Outcome Measures

Female Sexual Function Index (FSFI)

Sexual dysfunction criteria (FSFI score ≤26.55) improvement as defined as increased FSFI > 26.55 with treatment; baseline comparison made at the one-month and four-month post-treatment assessments.

Full Information

NCT ID

NCT04607798

First Posted

October 22, 2020

Last Updated

October 22, 2020

Sponsor

Venus Concept

1. Study Identification

Unique Protocol Identification Number

NCT04607798

Brief Title

Multi-polar RF and PEMF for Treatment of Vulvovaginal Atrophy

Official Title

Clinical Evaluation of the Safety and Efficacy of Using Multi-Polar RF and PEMF Technologies for the Treatment of Symptoms Associated With Vulvovaginal Atrophy

Study Type

Interventional

2. Study Status

Record Verification Date

October 2020

Overall Recruitment Status

Completed

Study Start Date

October 3, 2017 (Actual)

Primary Completion Date

May 31, 2020 (Actual)

Study Completion Date

May 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Venus Concept

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

5. Study Description

Brief Summary

The study evaluates the use of multi-polar radiofrequency (RF) and pulsed electro-magnetic fields (PEMF) energies for the treatment of symptoms related to genitourinary syndrome of menopause (GSM)/vulvovaginal atrophy (VVA). All subjects will receive a total of three internal treatments at four week intervals. Subjects will be followed up at one and four months after treatment is complete.

Detailed Description

Largely observed in the post-menopausal population, a significant subset of pre-menopausal and peri-menopausal women are also affected by symptoms associated with GSM, the etiology being similar in that there is an interruption in normal estrogen production resulting in a hypoestrogenic state. Symptoms related to GSM include vaginal dryness, decreased lubrication, decreased vaginal elasticity, irritation and discomfort of the vaginal and vulvar tissues in general that can affect sexual health. Traditional treatments, such as hormone replacement therapy (HRT), are often the treatment of choice however come with potential risks and many women are not suitable candidates, or have contraindications to its use. Development of new technologies to address these concerns is warranted. RF energy-based treatment for symptoms of GSM has been used with success to promote elasticity restoration and improve moisture of the vaginal mucosa, and is well established in literature for the treatment of facial and neck laxity, stress urinary incontinence and skin tightening of tissue. Several studies show favorable results with improvement of vaginal laxity and sexual function with RF treatment. The addition of pulsed electromagnetic field (PEMF) energy to multi-polar RF therapy has also been shown to enhance the results of the RF therapy. RF therapy has already been reported to be successful in treatment of symptoms related to elasticity restoration and improve moisture of the vaginal mucosa. This study will investigate whether adding PEMF to RF therapy is safe and efficacious for the treatment of symptoms related to GSM and sexual health.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Genitourinary Syndrome of Menopause, Vulvovaginal Atrophy, Menopause

Keywords

Genitourinary Syndrome of Menopause, Menopause, Multi-polar Radio Frequency, Pulsed Electromagnetic Field, Sexual Dysfunction, Vaginal Laxity

7. Study Design

Primary Purpose

Treatment

Study Phase

Not Applicable

Interventional Study Model

Single Group Assignment

Masking

None (Open Label)

Allocation

N/A

Enrollment

40 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Vulvovaginal treatment

Arm Type

Experimental

Arm Description

Internal vaginal treatment monthly for 3 treatments.

Intervention Type

Device

Intervention Name(s)

Radiofrequency and pulsed electro-magnetic fields treatment

Intervention Description

Radiofrequency and pulsed electro-magnetic fields treatment of the vaginal canal to maintain an internal temperature of approximately 42 C for the proximal thermometer and 45 C for the mid and distal thermometers for 15 minutes.

Primary Outcome Measure Information:

Title

Vaginal Health Index

Description

Time Frame

Six months

Title

Description

Clinician assessed improvement (reduction) in vaginal pH with baseline comparison made at the one-month and four-month post-treatment assessments.

Time Frame

Six months

Secondary Outcome Measure Information:

Title

Female Sexual Function Index (FSFI)

Description

Sexual dysfunction criteria (FSFI score ≤26.55) improvement as defined as increased FSFI > 26.55 with treatment; baseline comparison made at the one-month and four-month post-treatment assessments.

Time Frame

Six months

10. Eligibility

Sex

Female

Gender Based

Yes

Minimum Age & Unit of Time

19 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: Healthy female subjects, ≥19 years of age presenting with symptoms associated with GSM/VVA. Requesting treatment for vulvovaginal tissue for improvement of symptoms associated with GSM/VVA, with a score of ˂26.55 on the FSFI. Sexual activity (vaginal intercourse minimum twice per month) in a monogamous relationship. At least one full-term pregnancy (>36 weeks gestation) with vaginal delivery completed at least one year before study enrollment. Exclusion Criteria: Pregnant or intending to become pregnant during the course of study. Having any active electrical implant anywhere in the body, such as a pacemaker or an internal defibrillator. Having a permanent implant in the treated area (e.g. intrauterine device) Prior use of collagen, fat injections and/or other methods of skin augmentation (enhancement with injected or implanted material) in the treated area within 4-6 weeks of the initial treatment or during the course of the study. Use of retinoids such as oral Isotretinoin (Accutane®) within 6 months of initial treatment or during the course of the study. Any other surgery in treated area within 12 months of initial treatment or during the course of the study. Open laceration, abrasion, bleeding, infection or inflammation of any sort on or in the area to be treated. Active sexual transmitted disease (STD) (e.g. genital Herpes Simplex, condylomata) or vaginosis. Chronic vulvar pain or vulvar dystrophy. History of immunosuppression/immune deficiency disorders (including HIV infection or AIDS) or use of immunosuppressive medications, including corticosteroids, 6 months prior to and during the course of the study. Having any form of active cancer at the time of enrollment and during the course of the study. Significant concurrent illness, such as uncontrolled diabetes i.e. any disease state that in the opinion of the Investigator would interfere with the treatment, or healing process. Participation in a study of another device or drug within 1 month prior to study enrollment or during this study, and as per the Investigator's careful discretion, as long as not contradictory to any of the above criteria. Mentally incompetent or evidence of active substance or alcohol abuse. Having any stage 3-4 cystocele, rectocele, enterocele paravaginal defect or major pelvic organ prolapse beyond the hymenal ring. Unstable dosages of medications such as antihypertensives or psychotropics that are known to affect sexuality. Skin piercing in the treatment area. Tattoos in the treatment area. Prior skin treatment with laser in the treated area within 6 months of the initial treatment or during the course of treatment. Prior ablative resurfacing procedure in the treated area with laser or other devices within 12 months of the initial treatment or during the course of treatment. History of keloid formation or poor wound healing in a previously-injured skin area. History of epidermal or dermal disorders (particularly if involving collagen or microvascularity). Menstruation less than 7 days prior to treatment.

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

Matthew Gronski, PhD

Organizational Affiliation

Venus Concept

Official's Role

Study Director

Facility Information:

Facility Name

Cogerent Laser Clinics Group

City

Kyiv

ZIP/Postal Code

02002

Country

Ukraine

12. IPD Sharing Statement

Citations:

PubMed Identifier

34327510

Citation

Kolodchenko Y. Nonablative, Noncoagulative Multipolar Radiofrequency and Pulsed Electromagnetic Field Treatment Improves Vaginal Laxity and Sexual Function. Womens Health Rep (New Rochelle). 2021 Jul 27;2(1):285-294. doi: 10.1089/whr.2021.0020. eCollection 2021.

Results Reference

derived

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Multi-polar RF and PEMF for Treatment of Vulvovaginal Atrophy

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