Non-genital warts. Viral wart, unspecified
Conditions
Interventions
Intervention group: In each patient, after examining the warts and relative matching according to the size and location, some of the warts will be treated with topical furosemide and some with 10% KOH
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
7 Years to 60 Years
Inclusion criteria
Inclusion criteria: Having at least 2 non-genital and non-flat warts Satisfaction with the study Age between 7 and 60 years
Exclusion criteria
Exclusion criteria: Pregnant and beast feeder women Receive effective treatments for warts in the last 30 days Having underlying cardiovascular, pulmonary or renal disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of warts. Timepoint: At the beginning of the study, 4 and 8 weeks after the intervention. Method of measurement: Physical examination.;Diameter of warts. Timepoint: At the beginning of the study, 4 and 8 weeks after the intervention. Method of measurement: Clinical examination and measurement with caliper.;Height of warts. Timepoint: At the beginning of the study, 4 and 8 weeks after the intervention. Method of measurement: Clinical examination and measurement with caliper. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMehdi Amirnia
Tabriz University of Medical Sciences
Outcome results
None listed