Condyloma acuminatum
Conditions
Interventions
experimental group:Two-step irradiance schedule
Control group:Conventional therapy
Sponsors
The Affiliated Hospital of Xuzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Clinical diagnosed with condyloma acuminatum, 18 years old and over; 2.Warts located in the perianal area, distal urethra and external genitalia. 3.All patients are unfit and reluctant to undergo surgery for any reasons, and volunteered to participate in the study and ability to understand and the willingness to sign a written informed consent even when they were informed of alternatives. Patients are willing to pay for the treatment, and agreed to take a picture of the skin lesions.
Exclusion criteria
Exclusion criteria: 1.Patients have been treated with ALA-PDT and those who have applied any other impact study within 12 weeks; 2.Patients with other diseases that may affect the efficacy evaluation, such as other photodermatosis; 3.Patients taking phototoxic or photosensitive drugs within 12 weeks; 4.Patients with clinically and / or pathologically proven tumor invasion to other organs or tissues; 5.Patients with severe immune dysfunction; 6.Patients with scar constitution; 7.Patients with known skin photoallergy, porphyria or allergy to ALA, light or lidocaine; 8.Patients suffer from serious internal diseases, psychological and mental diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Complete response rate of lesions at 1 month after treatment; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain assessment;Follow up the recurrence of lesions; | — |
Countries
China
Contacts
Public ContactJiang Guan
The Affiliated Hospital of Xuzhou Medical University
Outcome results
None listed