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The Effect of oral probiotic to improve genitourinary syndrome of menopausal women

The Effect of oral probiotic to improve genitourinary syndrome of menopausal women

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250720001
Enrollment
28
Registered
2025-07-20
Start date
2025-07-08
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Genito-urinary symptom in menopause by pelvic examination, VMI and microbiome Menopause, probiotic, Genitourinary symptom in menopause, VMI, microbiome

Interventions

participants take probiotic 1 tab before morning, evening for 30 days, and take pervaginal examination to test Vaginal health index, vaginal maturation index and vaginal microbiome before and after ta
Experimental Dietary Supplement,Placebo Comparator No treatment

Sponsors

Faculty of Medicine Research Grant
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Menopause, age > 40 year include : surgical menopause, early menopause 2. amenorrhea > 12 months after Last menopause period 3. Genito-urinary symtpom occur at least 1 times in 1 month, 4. determine to use probiotic

Exclusion criteria

Exclusion criteria: 1. History of taking hormone or lubricant for improve symptom of menopause in last 6 months, 2. History of allergy of probiotic, 3. History to use about product of probiotic : yoghurt, probiotic within 2 weeks, 4. History of pelvic infection within 4 weeks, 5. Severe genitourinary symptoms by pelvic examination, test pH

Design outcomes

Primary

MeasureTime frame
Vaginal maturation index before and after take probiotic/placebo Cytology of vaginal epithelium

Secondary

MeasureTime frame
microbiome before and after take probiotic vaginal microbiome

Countries

Thailand

Contacts

Public ContactSappawit Lertlerphant

Chiangmai university

sappawitlert@gmail.com0863566567

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026