Condylomata Acuminata
Conditions
Interventions
This is a two-arm randomized clinical study. The study included female patients, between 18 and 60 years old, with a diagnosis of condyloma acuminata confirmed by clinical and, if necessary, histopath
C01.221.812.640.700
Sponsors
Universidade de São Paulo
Universidade Federal de São Carlos
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Female patients between 18 and 60 years old diagnosed with Condylomata Acuminata
Exclusion criteria
Exclusion criteria: Patients pregnant; lactating; immunologically suppressed; and those undergoing other treatment within less than 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effectiveness assessment of treatments and comparison between groups | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of lesions recurrence during up to 12 months of patients after treatments, the cosmetic result after 30 days, and the pain score during photodynamic therapy. | — |
Countries
Brazil
Contacts
Public ContactMirian Denise Stringasci
Universidade de São Paulo
Outcome results
None listed