Clinical Trial

Ultrasonographic Evaluation of Cosmetic Keratolytic Treatment of Foot Calluses and Corns

Completed
View on ClinicalTrials.gov →
Summary
This prospective, non-randomized, controlled study evaluated the efficacy of a topical cosmetic keratolytic preparation (serum and cream containing urea, salicylic acid, and collagen) in reducing the thickness and associated pain of hyperkeratotic foot lesions (calluses and corns). High-frequency ultrasonography (18 MHz) was used for precise, quantitative measurement of lesion thickness before and after a two-month intervention. Participants were allocated to four parallel groups (treated calluses, untreated callus controls, treated corns, and untreated corn controls).
Trial Details
NCT Number NCT07765225
Lead Sponsor Wroclaw University of Health and Sport Sciences
Conditions Hyperkeratosis, Callus, Corn (Clavus), Foot Dermatoses
Enrollment 124 participants
Start Date 2020-02-01
Primary Completion 2026-03-01 (estimated)
Study Completion 2026-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-14