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Randomized controlled study of mometasone furoate and tacrolimus in the treatment of vulvar lichen sclerosus

Randomized controlled study of mometasone furoate and tacrolimus in the treatment of vulvar lichen sclerosus

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102770
Enrollment
Unknown
Registered
2025-05-20
Start date
2023-05-05
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

vulvar lichen sclerosus

Interventions

Mometasone furoate treatment group:Local treatment with 0.1% mometasone furoate cream: once daily in the first month, and once every other day in the next month until the end of follow-up
Tacrolimus treatment group:Local treatment with 0.1% tacrolimus cream: once daily in the first month, and once every other day in the next month until the end of follow-up

Sponsors

Obstetrics and Gynecology Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients admitted to the Obstetrics and Gynecology Hospital of Fudan University between December 1, 2022 and December 31, 2024 with a diagnosis of VLS based on typical clinical signs and symptoms or histopathological examination.Complete clinical data.

Exclusion criteria

Exclusion criteria: Participants who received topical or systemic glucocorticoid or immunosuppressive therapy within 4 weeks prior to study participation Patients diagnosed with vulvar intraepithelial neoplasia or vulvar squamous cell carcinoma People with serious underlying diseases, including diabetes, heart, liver, and renal insufficiency, malignant tumors, and acquired immune deficiency syndrome Allergic to the investigational drug Pregnancy, lactation or family planning Poor mental condition, unable to cooperate with researchers Any ineligibility for inclusion in the study

Design outcomes

Primary

MeasureTime frame
Visual Analogue Score of Prutitus;

Secondary

MeasureTime frame
Skin color of vulva;Skin elasticity of vulva;

Countries

China

Contacts

Public ContactQing Cong

Obstetrics and Gynecology Hospital of Fudan University

qingcong@fudan.edu.cn+86 159 0079 8278

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026