Randomized, Controlled Trial With Hybrid Fractional Laser

You may be eligible if

• 1\. Healthy biological female aged between 40 to 70 years 2. Is post-menopausal with a AND b OR c:
• 1. No menses for at least 12 months
• 2. Follicle-stimulating hormone (FSH) level over 40mlU/mL
• 3. Has had a bilateral oophorectomy at least 12 months ago with no hormone replacement 3. Is experiencing at least two self-reported symptoms of GSM, such as
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• 1. Vaginal irritation in the absence of infection
• 2. Chronic burning sensation
• 3. Chronic itching in the absence of infection
• 4. Recurring urinary tract infections (UTIs)
• 5. Vaginal dryness during sexual activity
• 6. Pain during sexual activity (dyspareunia) 4. Has been experiencing symptoms of GSM for greater than 3 months 5. Is unable due to a medical contraindication or unwilling to receive hormone-based vaginal therapy 6. Early menopause after breast cancer 7. Normal and up to date pap smear, if applicable 8. Is sexually active (i.e. intravaginal intercourse) or has the potential and desire to be sexually active if symptoms of GSM improve 9. Can read, understand and sign informed consent form 10. Has indicated willingness to participate in the study by signing an informed consent form 11. Agrees to adhere to the treatment and follow-up schedule and post treatment care instructions