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Evaluation of the Efficacy of Intralesional Injection of Combined Digoxin and Furosemide Versus 5 - Fluorouracil in Treatment of Plantar Warts

S

Sohag University

Status

Enrolling

Conditions

Plantar Wart

Treatments

Drug: 5 fluorouracil
Drug: combined digoxin and furosemide

Study type

Interventional

Funder types

Other

Identifiers

NCT05520658
Soh-Med-22-07-01

Details and patient eligibility

About

Warts are common skin infections caused by human papillomavirus (HPV), which can cause a variety of skin presentations according to its type, site and the immune status .Nongenital warts may be presented as common, plane, plantar, filiform, or mucosal warts .Most people are affected by cutaneous warts, either plantar warts or common warts .prevalence of skin warts is between 3% and 13% and plantar warts are about 30% of skin warts in western world .Majority of cases occur in adolescent and young adults

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age:>18 years .
  • Sex: both males and females will be included.
  • Confirmed diagnosis by clinical and dermoscopic examination of plantar warts will be made

Exclusion criteria

  • Patients with history or evidenced hypersensitivity to any component used in this study.
  • Pregnancy & lactating.
  • Patients who receive immune suppressive therapy.
  • Patients who receive any wart treatment during the last 2 months before enrollment in the study.
  • Patients with systemic illness especially cardiac patients.
  • Patients who refused participation in the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

group A
Active Comparator group
Description:
patients will receive intralesional combined digoxin and furosemide , one session every 2 weeks for maximum 6 sessions
Treatment:
Drug: combined digoxin and furosemide
group B
Active Comparator group
Description:
patients will receive intralesional 5 fluorouracil mixed with 1ml of 2% lignocaine and epinephrine one session every 2 weeks for maximum 6 sessions .
Treatment:
Drug: 5 fluorouracil

Trial contacts and locations

1

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Central trial contact

samah R Ahmed, resident; Essam A Nada

Data sourced from clinicaltrials.gov

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