Clin2
NCT07737782Possibly a fitNot yet recruiting

Study of symptoms and quality of life for women with genitourinary syndrome of menopause

Vulvar AtrophyVulvovaginal Signs and SymptomsGenitourinary Syndrome of Menopause (GSM)Quality of LifeMenopause Related ConditionsDyspareuniaUrinary Incontinence, Urgency-frequencySexual Function

Part of Kidney & urinary, Mental health, Women’s health & pregnancy clinical trials.

This study looks at medical records of women with genitourinary syndrome of menopause (GSM) – a condition causing vaginal dryness, irritation, or urinary issues after menopause – who were treated with a product called XCM INTIM. The goal is to see how their symptoms and quality of life changed after at least 8 weeks of treatment.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
100 people
Ages
40 years to 75 years
Study type
Observational

Who can take part

  • You are a woman who has gone through menopause (no period for at least 12 months)
  • You have at least one symptom of genitourinary syndrome of menopause (like vaginal dryness, burning, or urinary problems) that affected your quality of life
  • You were treated with XCM INTIM and had a check-up at least 8 weeks after starting treatment
  • You were seen at the Hospital Universitario La Luz in Madrid between January 2022 and April 2026
  • You did not use any vaginal hormone products 4 weeks before starting XCM INTIM, or systemic estrogen therapy 8 weeks before
  • You did not have other gynecological or urinary conditions (like active infections, pelvic organ prolapse stage III or higher, or severe stress incontinence) that could confuse the results

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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