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Vaginal suppository versus oral capsule of vitamin D for vaginal atrophy in postmenopausal women; A randomized controlled trial.

Vaginal suppository versus oral capsule of vitamin D for vaginal atrophy in postmenopausal women; A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210224004
Enrollment
72
Registered
2021-02-24
Start date
2021-02-25
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

vaginal atrophy in postmenopausal women Vaginal vitamin D vaginal atrophy postmenopausal women vitamin D

Interventions

vitaminD3 1000IU vaginal suppository once daily for 8 weeks ,vitaminD3 1000IU oral administration once daily for 8 weeks
Active Comparator Drug,Active Comparator Drug
vaginal suppository,oral administration

Sponsors

Faculty of Medicine Khon kaen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Woman with vaginal atrophy age 45 years old or more who had amenorrhea for at least 1 year or underwent bilateral oophorectomy or who had serum FSH more than 40 IU/ml

Exclusion criteria

Exclusion criteria: 1. who had history hormonal replacement therapy or vitamin D3 used for 12 weeks before enrollment 2. who had abnormal vaginal bleeding for 12 weeks before enrollment 3. who had history used any vaginal suppository or vaginal apply for 4 weeks before enrollment 4. who had history of sexual transmitted disease 5. who had abnormal pap smear 6. hypersensitivity to vitamin D 7. liver or renal failure 8. who had high serum phosphate

Design outcomes

Primary

MeasureTime frame
the most bothersome symptoms of vaginal atrophy 4 and 8 weeks after intervention severity of symptoms

Secondary

MeasureTime frame
vaginal maturation value 4 and 8 weeks after intervention vaginal maturation value,vaginal pH 4 and 8 weeks after intervention vaginal maturation value,satisfactory 8 weeks after intervention rating scale

Countries

Thailand

Contacts

Public ContactPakapong Kerdtawee

Faculty of Medicine Khon Kaen University

pkp.rm@hotmail.com0961415142

Outcome results

None listed

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