A Randomised Controlled Trial of Precision diagnosis and treatment of Lichenoid vulvar disease

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000037349

Enrollment

Unknown

Registered

2020-08-28

Start date

2020-10-01

Completion date

Unknown

Last updated

2020-10-19

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

Conditions

Lichenoid vulvar disease

Interventions

Patients with chronic simple lichenification of the vulva research group:Fractional laser treatment

Patients with chronic simple lichenification of the vulva Control group:Topical corticosteroid therapy

Study group of patients with vulvar lichen sclerosus-1:Fractional laser treatment

Study group of patients with vulvar lichen sclerosus-2:Photodynamic therapy

Control group of patients with vulvar lichen sclerosus:Topical corticosteroid therapy

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: (1) Patients with vulvar lichenosis were diagnosed clinically and histopathologically confirmed in our hospital. (2) Women aged 18-90 years old.

Exclusion criteria

Exclusion criteria: (1) Patients with vulvar cancer; (2) Patients with acute vulvitis, vaginitis, and pelvic inflammatory disease.

Design outcomes

Primary

Measure	Time frame
Treatment effect;	—

Countries

China

Contacts

Public ContactSUI Long

Obstetrics and Gynecology Hospital of Fudan University

suilong@fudan.edu.cn+86 13801788118

Outcome results

None listed

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