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Effectiveness of vaginal estriol with lactobacilli on urinary symptoms in postmenopausal women: a randomized-controlled trial

Effectiveness of vaginal estriol with lactobacilli on urinary symptoms in postmenopausal women: a randomized-controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210623003
Enrollment
76
Registered
2021-06-23
Start date
2021-07-05
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary tract symptoms in postmenopausal women Lower urinary tract symptoms Administration, Intravaginal Estriol

Interventions

Estriol 0.03 mg plus Lactobacillus acidophilius vaginal tablet,Placebo composed of microcrystalline cellulose, magnesium stearate and silicon dioxide
Experimental Drug,Placebo Comparator Drug
vaginal estriol plus lactobacilli,Placebo

Sponsors

Khon Kaen University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Postmenopausal women with urinary tract symptoms (frequency or urgency or dysuria or nocturia or stress urinary incontinence or urgency urinary incontinence)

Exclusion criteria

Exclusion criteria: Previous vaginal or urethral surgery or hysterectomy, Pelvic organs prolapsed stage 3-4, History of endometrial hyperplasia or cancer, History of breast cancer, Undiagnosed AUB, Allergic reaction to vaginal tablet, History of vaginal estrogen or systemic estrogen use in previous month, History of muscarinic antagonist or beta-3 adrenergic agonist in previous month, Currently using the vaginal pessary, BMI exceeding 25 kg/m*m, Cannot understand Thai language, Deny participation

Design outcomes

Primary

MeasureTime frame
Improvement of urinary tract symptoms at the end of the study visual analog scale

Secondary

MeasureTime frame
Mean symptoms score at the end of the study Visual analog scale,Quality of life at the end of the study IIQ-7,Satisfaction at the end of the study Visual analog scale,Adverse effect at the end of the study Questionnaire

Countries

Thailand

Contacts

Public ContactApiwat Jongjakapun

Khon Kaen University

apiwjo@kku.ac.th66634073183

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026