Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
COMPLETED
NCT07765225
NA

Ultrasonographic Evaluation of Cosmetic Keratolytic Treatment of Foot Calluses and Corns

Sponsor: Wroclaw University of Health and Sport Sciences

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).

Official title: Ultrasonographic Evaluation of Cosmetic Keratolytic Treatment of Hyperkeratotic Foot Lesions: A Prospective, Non-randomized, Controlled, Comparative Study of Calluses and Corns

Key Details

Gender

FEMALE

Age Range

35 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

124

Start Date

2020-02-01

Completion Date

2026-05-01

Last Updated

2026-08-14

Healthy Volunteers

No

Interventions

OTHER

Topical Keratolytic Cosmetic (Serum + Cream)

Application of 2 mL serum followed by 2 mL cream containing urea, salicylic acid, and collagen, massaged into the hyperkeratotic lesion for 2 minutes, twice daily (morning and evening) for 2 months

Locations (1)

OSTEON Clinic

Swidnica, Poland