Based on the patient reported outcome (PRO), the study on the postoperative symptom management system for the treatment of vulvar leukoplakia with focused ultrasound was established

Authors
Category Primary study
Registry of TrialsChinese Clinical Trial Register
Year 2024
INTERVENTION: 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; CONDITION: Leukoplakia vulva PRIMARY OUTCOME: Subjective evaluation of CSS score; SECONDARY OUTCOME: Clinician objective CSS score;Cattaneo clinical signs and symptoms score;EQ‐5D‐5L Health Questionnaire; 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.
Epistemonikos ID: 24ad64e22c361d863277d32190c2decf8cea4d2a
First added on: Apr 08, 2025