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A randomized controlled trial of platelet-rich plasma therapy for lichenoid vulvar disease

A randomized controlled trial of platelet-rich plasma therapy for lichenoid vulvar disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097528
Enrollment
Unknown
Registered
2025-02-20
Start date
2025-02-27
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

lichenoid vulvar disease

Interventions

Sponsors

West China Second Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1. Patients with a confirmed clinical and/or pathological biopsy diagnosis of VLD; 2. No relevant treatment received in the past two weeks; 3. Complete clinical and pathological data, with follow-up compliance; 4. Willingness to participate in the study and signed informed consent.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: 1. History of protein allergy; 2. Acute inflammatory phase of the genitourinary system; 3. Presence of hematologic disorders, immune dysfunction, or malignancies; 4. Pregnancy; 5. Severe systemic medical conditions affecting daily life (e.g., diagnosed severe cardiovascular diseases or immune system disorders); 6. Psychological or psychiatric disorders (e.g., depression) that prevent completion of follow-up.

Design outcomes

Primary

MeasureTime frame
Treatment efficacy rate;Degree of symptom improvement;Dermatology Life Quality Index (DLQI);

Secondary

MeasureTime frame
Subjective patient satisfaction;Incidence of adverse reactions;

Countries

China

Contacts

Public ContactWei Dongmei

West China Second Hospital of Sichuan University

weidongmei@scu.edu.cn+86 189 8215 0655

Outcome results

None listed

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