Skip to main content
Clinical Trials/NCT06780163
NCT06780163CompletedPhase 4

A Pre-Post Quasi-Experimental Study to Evaluate the Effects of Vaginal Estrogen on the Urine Microbiome and Overactive Bladder Symptoms in Menopausal Women

Mahidol University1 site in 1 country30 target enrollmentStarted: June 27, 2025Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Change in Lactobacillus abundance

Study Overview

Brief Summary

The goal of this Pre-Post Quasi-experimental study is to investigates the effect of vaginal estrogen therapy on changes in the urinary microbiome and its association with improvement in overactive bladder (OAB) symptoms in menopausal women

Primary Objective:

To evaluate the effects of vaginal estrogen on the level of Lactobacillus in the urine of postmenopausal women with OAB.

Secondary Objectives

  1. To evaluate the effects of vaginal estrogen on urine microbiome in postmenopausal women with OAB.
  2. To identify the association of alterations of urine microbiome after vaginal estrogen treatment with overactive bladder symptoms.

After informed and consents process, urine samples for microbiome study will be collected from participants with sterile technique. 17β-estradiol 10 mcg will be given to the participants. The participants will be ask to use 1 tab daily for 2 weeks vaginally before bed, then 1 tab twice a week vaginally before bed until 12 weeks. Then they will come back to hospital to take urine sample for microbiome study.

Detailed Description

Overactive bladder (OAB) is a common condition affecting 12-20% of adults, particularly women in the menopausal phase. OAB is characterized by urinary urgency, frequency, nocturia, and sometimes urgency urinary incontinence, significantly impairing quality of life. Menopause is associated with a decline in estrogen levels, which affects the integrity of the lower urinary tract and may contribute to OAB symptoms.

Vaginal estrogen therapy has been used to alleviate urogenital symptoms in postmenopausal women by improving vaginal atrophy, enhancing urethral closure pressure, and potentially improving bladder function. Recent studies have suggested that the urinary microbiome plays a critical role in urinary tract health and dysfunction. Alterations in the urinary microbiome, known as dysbiosis, have been linked to conditions such as OAB, urgency urinary incontinence, and recurrent urinary tract infections.

This pre-post quasi-experimental study aims to evaluate the effects of vaginal estrogen therapy on the urinary microbiome and its association with OAB symptom improvement in menopausal women. Specifically, the study will focus on:

  1. Measuring changes in Lactobacillus abundance in urine after vaginal estrogen therapy. (Primary objective)
  2. Measuring changes in the overall urinary microbiome diversity. (Secondary objective)
  3. Identifying associations between changes in the microbiome and improvements in OAB symptoms. (Secondary objective)

The study will enroll 30 postmenopausal women with a clinical diagnosis of OAB who meet specific inclusion criteria. Participants will receive 17β-estradiol vaginal tablets (10 mcg) daily for the first two weeks, followed by twice-weekly doses for a total of 12 weeks. Urine samples will be collected via sterile catheterization at baseline and after 12 weeks to analyze microbiome diversity and Lactobacillus levels. OAB symptoms will be assessed using validated Thai versions of the Overactive Bladder Symptom Score (OABSS) and Overactive Bladder Questionnaire Short Form (OAB-q SF).

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Natural or surgical menopause at least 1 year
  • •Present with overactive bladder symptoms by using validated Thai version of OVERACTIVE BLADDER SYMPTOM SCORE (score in No.3 ≥ 2 and overall score ≥ 3)
  • •Absence of urinary infection
  • •Post-void residual urine less than 100ml

Exclusion Criteria

  • •Currently or prior use of systemic hormone replacement therapy or vaginal estrogen within the past 3 months
  • •Contraindication or allergy to estrogen therapy
  • •Use of antibiotics, prebiotics and probiotics within the past 2 weeks
  • •Currently on antimuscarinic or β3 agonists medication or within the past 3 months
  • •Pelvic organ prolapse greater than stage II

Arms & Interventions

Estrogen

Experimental

Participants will receive 17β-estradiol vaginal tablets (10 mcg) daily for the first two weeks, followed by twice-weekly doses for a total of 12 weeks. Participants will be asked to bring the blister pack for pill count at the 12-week follow-up (checking for compliance)

Intervention: 17β-estradiol 10 mcg (Drug)

Outcomes

Primary Outcomes

Change in Lactobacillus abundance

Time Frame: From enrollment to the end of treatment at 12 weeks

Change in Lactobacillus abundance (measure by urine microbiome study) after vaginal estrogen therapy

Secondary Outcomes

  • Change in urine microbiome diversity(From enrollment to the end of treatment at 12 weeks)
  • Association of change in urine microbiome with overactive bladder symptoms(From enrollment to the end of treatment at 12 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials