Clinical efficacy of focused ultrasound combined with Shenju lotion in the treatment of vulvar intraepithelial non neoplastic lesions

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000037618

Enrollment

Unknown

Registered

2020-08-29

Start date

2020-09-01

Completion date

Unknown

Last updated

2020-11-02

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

Conditions

Intraepithelial neoplasia of vulva

Interventions

experimental group:Treatment of focused ultrasound combined with Shenju Lotion

control group: focused ultrasound

Eligibility

Sex/Gender

Female

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. All the patients met the diagnostic criteria of vulvar intraepithelial non neoplastic lesions and were confirmed by vulvar biopsy. 2. Patients did not receive other treatment before participating in this study. 3. Patients and their families voluntarily signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Menstrual period, pregnancy and lactation period; 2. The medical records are defective or unknown; 3. Vulvar cancer, vulvar precancerous lesions, acute vulvar or vaginal infection; 4. Systemic diseases or diabetes.

Design outcomes

Primary

Measure	Time frame
vascular endothelial growth factor;Endothelin-1;pruritus;	—

Countries

China

Contacts

Public ContactWang Lei

Gansu Hospital of Traditional Chinese Medicine

948629023@qq.com+86 13919862168

Outcome results

None listed

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