Prospective, Open-Label, Single-Center, Non-Comparative Study to Assess the Use of Pixel CO2 Laser System (FemiLift) in the Treatment of Vulvovaginal Atrophy (VVA) in Postmenopausal Female Subjects

Inclusion criteria

• Healthy, non-smoking
• Woman, age 35 to 70 yrs, menopausal
• Provided written Informed Consent
• Exhibiting VVA and/or SUI symptoms (mild or moderate SUI, according to severity index developed by Sandvik.)
• Prolapse staged < II, according to the pelvic organ prolapse quantification (ICS-POP-Q) system
• Normal PAP smear (up to 1 year prior to baseline)
• Vaginal canal, introitus and vestibule free of injuries and bleeding
• 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

• Severe prolapse (POP>= grade 3)
• Use of photosensitive drugs
• Acute or recurrent urinary tract infection (UTI), or genital infection (e.g. herpes candida).
• Any serious disease, or chronic condition, that could interfere with the study compliance
• Acute or actively present within the last 2 months HPV/HSV
• Undiagnosed vaginal bleeding
• Urge or overflow incontinence
• Patients who are on antidepressants, or α-adrenergic and anticholinergic medications
• Patients with immune system diseases.
• Patients with allergic reaction to laser.
• Obese women (BMI >30)
• Patient unable to follow post-treatment instructions
• History of keloid formation
• Received or is anticipated to receive antiplatelets, anticoagulants, thrombolytics, vitamin E or anti inflammatories within 2 weeks pre treatment
• A history of thrombophlebitis
• A history of acute infections
• A history of heart failure
• Previously undergone reconstructive pelvic surgery
• Have used vaginal creams, moisturizers, lubricants or homeopathic preparations for at least 3 months
• Any medical condition that in the investigators opinion would interfere with the patients participation in the study