Leukoplakia vulva
Conditions
Interventions
Patient self-reported outcome group:Based on the patients self-reported symptoms, the doctor intervenes according to the symptoms
Conventional group:No intervention, routine follow-up
Sponsors
Nanchong Central Hospital
Eligibility
Sex/Gender
Female
Age
20 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Women with symptoms of vulvar leukoplakia; 2. Vulvar biopsy confirmed vulvar leukoplakia; 3. Able and willing to fill in the electronic scale through mobile phone or tablet computer.
Exclusion criteria
Exclusion criteria: 1. Inoperable patients with serious diseases; 2. Vulvar biopsy confirmed malignancy; 3. Those who cannot understand the research content; 4. The subject seriously violated the study plan (continued failure to follow the doctor's advice, intentionally asked the agent to fill out the forms, and intentionally provided wrong PRO information); 5. The subjects themselves asked to withdraw from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Subjective evaluation of CSS score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinician objective CSS score;Cattaneo clinical signs and symptoms score;EQ-5D-5L Health Questionnaire; | — |
Countries
China
Contacts
Public ContactTang Ying
Nanchong Central Hospital
Outcome results
None listed