Intralesional Injection of Combined Digoxin and Furosemide Versus 5-Flurouracil in Plantar Warts
Plantar Wart
About this trial
This is an interventional treatment trial for Plantar Wart
Eligibility Criteria
Inclusion Criteria: Patients with multiple plantar warts (≥ 3) will be included. Exclusion Criteria: Patients under 18 years old or patients over 65 years old. Pregnancy or breast feeding. Patients received vaccination or any other treatment of warts during the last month. Patients with a known sensitivity to any of the investigational product ingredients. Patients with history of asthma, allergic skin disorders or convulsions. Patients with signs of any systemic or local inflammation or infection. Patients with any evidence of immunosuppression including HIV. History of cardiac diseases, relevant abnormal K level or ECG abnormalities for patients who will receive the combined digoxin and furosemide.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Placebo Comparator
Group A
Group B
Group c
15 patients will receive intralesional 0.1 mL of combined digoxin and furosemide, with maximum 5 warts per session.
15 patients will receive intralesional injection of 5- Fluorouracil (50mg/ml) in full concentration into the wart using a 27- gauge insulin syringe till the entire lesion begins to puff up. The maximum dose injected per session will be 2ml of 5-FU.
15 patients will receive intralesional saline.