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17% Salicylate Versus 17% Salicylate-Ethyl Pyruvate for Plantar Foot Warts

G

Grossman, Michael, D.P.M.

Status and phase

Unknown
Phase 4

Conditions

Warts

Treatments

Drug: 17% Salicylate with ethyl pyruvate
Drug: Salicylates

Study type

Interventional

Funder types

Other

Identifiers

NCT01712295
R12-3128

Details and patient eligibility

About

Plantar warts on the sole of the foot are among the most common warts seen in podiatry clinics. Some patients are readily cured by simple standard of care treatments that include wart debridement (trimming or excision) and application of 17% salicylate (commercially known as Compound W)or by other treatments that may be painful and affect mobility. No treatment is consistently effective and most patients fail treatment multiple times.

Ethyl pyruvate (EP)is a common food additive noted to be 'generally regarded as safe' that may improve the activity of salicylate in wart treatment by improving the ability to penetrate and/or persist in the skin. The use of 17% salicylate with the addition of EP may improve cures of common foot plantar warts in subjects who also be receiving other standard-of-care treatment.

Enrollment

100 estimated patients

Sex

All

Ages

12 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • evidence of skin plantar wart(s)

Exclusion criteria

  • iodine allergy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 2 patient groups

17% Salicylate with Ethyl Pyruvate
Experimental group
Description:
Subjects with plantar wart(s) will apply the product to warts twice a day for up to 16 weeks.
Treatment:
Drug: 17% Salicylate with ethyl pyruvate
17% salicylate
Active Comparator group
Description:
subjects will apply 17% salicylate (standard of care treatment) to plantar skin wart(s) twice a day for up to 16 weeks
Treatment:
Drug: Salicylates

Trial contacts and locations

1

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Central trial contact

Michael Grossman, DPM

Data sourced from clinicaltrials.gov

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