CompletedPhase 3ACTRN12606000176561

Effectiveness of debridement of painful plantar calluses in older people

Effectiveness of scalpel debridement for the treatment of painful plantar calluses in older people: a randomised trial evaluating pain, plantar pressures and functional ability


Sponsor

Dr Karl B Landorf

Enrollment

80 participants

Start Date

May 15, 2006

Study Type

Interventional

Conditions

Summary

The aim of this project is to evaluate the effectiveness of reducing painful callus (hard skin) on the bottom of the feet (using scalpel debridement) versus no reduction (using a sham debridement technique). This study is double-blind: both the participants and the assessors will be blinded.


Eligibility

Sex: Both males and femalesMin Age: 65 YearssMax Age: 80 Yearss

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying: Effectiveness of debridement of painful plantar calluses in older people. It may be open to adults aged 65 to 80 who meet certain criteria, including: Have painful plantar forefoot callus that has not been treated in the past 6 weeks•Callus must register at least 20mm on a 100mm visual analogue scale. Participation typically involves medical assessments, possible treatment with the study intervention, and follow-up visits to track your health.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Scalpel debridement versus sham scalpel debridement of plantar callus The intervention period is six weeks. (Scalpel debridement = removal or reduction of the callus by using a scalpel or sharp blad

Scalpel debridement versus sham scalpel debridement of plantar callus The intervention period is six weeks. (Scalpel debridement = removal or reduction of the callus by using a scalpel or sharp blade)


Locations(1)

VIC, Australia

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ACTRN12606000176561