Fractional Handpiece With CO2 Laser: Fractional Ablative Laser Treatment of Vulvovaginal Atrophy

Vulvovaginal Atrophy Clinical Trial

Official title:

Fractional Handpiece With CO2 Laser: Fractional Ablative Laser Treatment of Vulvovaginal Atrophy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03271944
• Other study ID #: 20161370
• Status: Recruiting
• Phase: N/A
• First received: August 29, 2017
• Last updated: March 22, 2018
• Start date: December 29, 2016
• Est. completion date: December 2019

Study information

• Verified date: March 2018
• Source: The American Association of Female Pelvic Medicine Specialists, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To assess the feasibility and efficacy of the CO2 fractional handpiece in the treatment of vulvovaginal atrophy (VVA) in post-menopausal women and its effect on the patient VHIS(vaginal health index core). The primary endpoint is to assess the change in the vaginal dryness by means of a visual analogic scale (10 cm VAS).

Description:

The purpose of this study is to evaluate the use of a CO2 laser (EdgeTM CO2 Laser) with a fractional handpiece made specifically for the vagina to possibly restore the normal physiological conditions of the vagina, thus reducing the symptoms of VVA. The EdgeTM CO2 Laser and general fractional handpiece is approved by the FDA for ablative skin resurfacing (for example, treating fine lines and wrinkles, acne and surgical scars, skin pigmentation and discoloration, sun damage, pre-cancerous as well as benign lesions and uneven skin texture). The fractional handpiece used in this study for the treatment of VVA is experimental and has not been approved by the FDA for vaginal dryness associated with menopause.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: December 2019
• Est. primary completion date: December 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 40 Years to 80 Years

Eligibility

Inclusion Criteria:

• Subjects meeting the following inclusion criteria may participate:

• Healthy non-smoking post menopausal women with absence of menstruation of at least 12 months

• Exhibiting VVA symptoms

• Prolapse staged < II, according to the pelvic organ prolapse quantification (ICS-POP- Q) system

• Have not had procedures in the anatomical area through 6 months prior to treatment

• Understand and accept the obligation and is logistically able to present for all scheduled follow-up visits

Exclusion Criteria:

• Subjects meeting any of the following criteria will be excluded from participation:

• Acute or recurrent urinary tract infection (UTI), or genital infection (e.g. herpes candida).

• Prolapse staged = II, according to the pelvic organ prolapse quantification (ICS-POP- Q) system

• Any serious disease, or chronic condition, that could interfere with the study compliance

• Previously undergone reconstructive pelvic surgery

• Have used vaginal creams, moisturizers, lubricants or homeopathic preparations for at least 3 months

• A history of thrombophlebitis

• A history of acute infections

• A history of heart failure

• Received or is anticipated to receive antiplatelets, anticoagulants, thrombolytics, vitamin E or anti inflammatories within 2 weeks pre treatment

• Any medical condition, that, in the investigator's opinion would interfere with the patient's participation in the study

• Taking medications that are photosensitive

• A history of keloid formation

Related Conditions & MeSH terms

• Atrophy
• Vulvovaginal Atrophy

Intervention

Device:
• CO2 Laser Treatment
Fractional handpiece with CO2 laser: Fractional Ablative laser Treatment of Vulvovaginal Atrophy

Locations

Country	Name	City	State
United States	The American Association of Female Pelvic Medicine Specialists, Inc.	Agoura Hills	California

Sponsors (2)

Lead Sponsor	Collaborator
SHERRY Thomas	Perigree Medical

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Fractional handpiece with CO2 laser: Fractional Ablative laser Treatment of Vulvovaginal Atrophy (VVA).	The purpose of this study is to evaluate efficacy and safety of CO2 laser (EdgeTM CO2 Laser) with a fractional headpiece in the treatment of vulvovaginal atrophy (VVA) in post- menopausal women and its effect on the patient VHIS (vaginal health index score). The primary endpoint is to assess the changes in the vaginal dryness by mean of a visual analog scale (10 cm VAS).	9 month