Actively Recruiting

Phase Not Applicable
Age: 45Years - 65Years
FEMALE
NCT06726746

Efficacy of Fractional CO2 Laser Treatment in Post-Menopausal Women With Vaginal Atrophy

Led by Cairo University · Updated on 2024-12-10

20

Participants Needed

1

Research Sites

73 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Vaginal dryness, itching, burning, irritability, secretion, and various urinary problems are the symptoms of vulvovaginal atrophy. Therefore, more attention must be paid to relieve these symptoms in order to provide better sexual health for postmenopausal women. At present, an accumulating body of evidence suggests safety and efficacy of laser and energy-based devices for the treatment of women's genitourinary conditions. More clinical studies are needed to assess the safety profile and clinical outcomes of the lasers and energy-based devices to treat the symptoms associated with vulvovaginal atrophy (VVA)

CONDITIONS

Official Title

Efficacy of Fractional CO2 Laser Treatment in Post-Menopausal Women With Vaginal Atrophy

Who Can Participate

Age: 45Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 45 to 65 years who are menopausal
  • Currently sexually active
  • Experiencing symptoms of vulvovaginal atrophy such as vaginal dryness, irritation, soreness, or pain during intercourse
Not Eligible

You will not qualify if you...

  • Hormonal therapy use within the past 6 months
  • Use of vaginal moisturizers or lubricants within the past 30 days
  • Acute or recurrent urinary tract infections
  • Active genital infections
  • Pelvic organ prolapse stage II or higher
  • Psychiatric disorders
  • Undiagnosed vaginal bleeding
  • Serious diseases or chronic conditions that could interfere with study participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cairo University

Cairo, Egypt

Actively Recruiting

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Research Team

D

Daniel Onsi

CONTACT

M

Mohammed El-Noury

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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