vulva white lesion
Conditions
Interventions
Experimental group:Guiqitengcao ointment
control group:Bamboo myxin ointment
Sponsors
Beijing University of TCM
Eligibility
Sex/Gender
Female
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: (1) patients who meet the above diagnostic criteria of western medicine and are diagnosed with white vulva lesion; (2) those who meet the above diagnostic criteria of TCM and are diagnosed as pruritus vulvae of blood deficiency and hygroscopic; (3) women aged between 20 and 60 years; (4) those who have not used traditional Chinese medicine for the treatment of this disease in the last 1 month, and those who have not used hormone drugs in the last 3 months; (5) voluntarily participate in this clinical study and sign the informed consent.
Exclusion criteria
Exclusion criteria: (1) squamous vulvar intraepithelial neoplasia;Vulva cancer, vitiligo, albinism; (2) women during pregnancy and lactation; (3) acute and chronic vulva vaginal infection; (4) diabetics; (5) severe cardiovascular and cerebrovascular diseases or abnormal liver and kidney functions. (6) participating in other clinical trials within 3 months; (7) malformed reproductive organs; (8) people with allergic constitution or mental disorder or who do not have personal ability to act.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Itching degree;Clinical symptoms;Clinical signs; | — |
Secondary
| Measure | Time frame |
|---|---|
| TCM syndrome score; | — |
Countries
China
Contacts
Public ContactQing Tong
Dongfang Hospital Affiliated to Beijing University of TCM
Outcome results
None listed