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Er:YAG Laser Combined With Vaginal Estriol for Genitourinary Syndrome of Menopause

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Study description expanded, about 82 wordsv5
  2. Minor Study description expanded, about 12 words
    • Study title shortened, about 1 word
    v4
  3. Notable Trial status: Not Yet Recruiting to Recruitingv3 Show 8 more changesShow less
    • Primary completion date: May 10, 2026 to Nov 10, 2026
    • Study completion date: Jul 20, 2026 to Dec 31, 2026
    • Interventions: Laser Er:YAG Off (Radiation), Laser Er:YAG On (Radiation), Topical estrogen therapy based on estriol (E3) (Drug) to Active Er:YAG Laser (Radiation), Sham Er:YAG laser (minimal fluence) (Radiation), Topical estrogen therapy based on estriol (E3) (Drug)
    • Eligibility criteria shortened, about 51 words
    • Secondary endpoints: 5 to 4
    • Study description expanded, about 74 words
    • Site details revised
    • Study title shortened, about 2 words
  4. Notable Primary completion date: Jul 20, 2025 to May 10, 2026
    • Start date: Mar 26, 2025 to Dec 10, 2025
    • Study completion date: Aug 30, 2025 to Jul 20, 2026
    • Secondary endpoints: details revised at 4 of 5 entries
    v2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Chronic hypoestrogenism in postmenopausal women significantly impacts the urogenital epithelium, leading to Genitourinary Syndrome of Menopause (GSM) and increasing susceptibility to gynecological infections due to vaginal pH elevation. Therapies using the Erbium:YAG (Er:YAG) 2940nm laser and low dose topical estrogen have demonstrated efficacy in improving vaginal trophism and restoring microbiota balance. This randomised, double-blind clinical study aims to assess the effects of combining Er: YAG laser therapy with vaginal estriol compared with estriol therapy alone in postmenopausal women with GSM. Sixty patients will be recruited and randomly assigned to two groups. All participants will receive low-dose topical estrogen therapy (estriol cream ) for 14 days, followed by twice-weekly applications until completing three laser sessions at four-week intervals. Group 1 (Sham) will receive the laser with minimal fluence (0.5J/cm²) applied to maintain blinding (auditory cues) below the threshold for biological tissue, while Group 2 , will undergo active laser treatment. Inclusion criteria include age 45-70 years, vaginal pH ≥5, absence of hormone therapy or energy-based intimate treatments for 180 days, and moderate vaginal atrophy symptoms (SCORE \>4). Exclusion criteria include abnormal cervicalvaginal cytology in the last six months, corticosteroid therapy within 90 days, and BMI ≥35kg/m². Assessments will occur at Baseline, 30 days after each laser session and 4 months after the third laser application. The primary outcome is the Vaginal Health Index (VHI), while secondary outcomes include GSM symptom evaluation via the Visual Analog Scale, vaginal microbiota analysis through 16S gene sequencing, and quality-of-life and sexual health questionnaires. Statistical analysis of the groups will be performed using SPSS version 22.0. For analytical statistics, repeated measures ANOVA will be used for continuous data, and non-parametric tests for repeated measures, such as the Friedman test, when appropriate. A p-value \<0.05 will be considered statistically significant.
Trial Details
NCT Number NCT06873971
Lead Sponsor University of Nove de Julho
Conditions
(from sponsor)
Genitourinary Syndrome of Menopause
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov