Clinical Trials Directory

Trials / Completed

CompletedNCT07307131

Furosemide-Digoxin vs. Polidocanol for Cutaneous Warts

A Head-to-Head Comparison of Intralesional Furosemide-Digoxin Versus Polidocanol for the Treatment of Cutaneous Warts With 6-Month Follow-up

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
64 (actual)
Sponsor
Benha University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study compares the effectiveness and safety of two different intralesional treatments for cutaneous warts: a combination of furosemide and digoxin versus polidocanol.

Detailed description

This is a prospective, randomized, single-blind, comparative clinical study to evaluate the efficacy and safety of intralesional combined furosemide-digoxin versus intralesional polidocanol in the treatment of cutaneous warts. Sixty-four adult patients were randomized to receive one of the two treatments every two weeks for a maximum of four sessions. The main goal was to see which treatment was better at completely clearing the warts. The study also looked at side effects and how often the warts came back within six months.

Conditions

Interventions

TypeNameDescription
DRUGIntralesional combined furosemide (10 mg/ml) and digoxin (0.25 mg/ml)Group A (Experimental): Intralesional combined furosemide (10 mg/ml) and digoxin (0.25 mg/ml)
DRUGIntralesional polidocanol 2%Group B (Active Comparator): Intralesional polidocanol 2%

Timeline

Start date
2024-09-01
Primary completion
2025-03-01
Completion
2025-09-30
First posted
2025-12-29
Last updated
2026-01-02

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07307131. Inclusion in this directory is not an endorsement.