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Fuzzy Wale Compression Stockinet to Promote Healing Following Transtibial Amputation for Peripheral Arterial Disease

A Pilot Study of Fuzzy Wale Compression Stockinet to Evaluate Healing Following Transtibial Amputation for Peripheral Arterial Disease

Who can join

Ages 18 and older · All sexes

Inclusion Criteria:

* \>18 years
* Male and female
* Transtibial amputation expected.
* Peripheral arterial disease and Transcutaneous partial pressure of oxygen (TCP02, if performed)
* Ability of subject to give appropriate consent or have an appropriate representative available to do so.

Exclusion Criteria:

* Known allergies to any of the components of the compression.
* Terminal illness or current cancer therapy with chemotherapy
* Inability to undergo ongoing care in Rochester.
* Lack of cognitive ability to follow instructions or monitor residual limb.
* Vulnerable study population
* Pregnancy

About the study

The objective of this study is to determine if using Fuzzy Wale compression stockinet can assist in reducing the healing time and decrease costs in transtibial amputation patients as compared to standard of care treatment compression stocking.

What is being tested

• Fuzzy Wale Compression Stockinet (device)

Sponsor: Mayo Clinic · Participants: 40 · Started: Jul 7, 2025

Contact the study team

• Vascular Research Team · Phone: (507) 538-7425
• Matthew Melin, M.D. · Phone: (507) 266-6717

Official record on ClinicalTrials.gov — NCT06308562

Locations in the U.S.

Conditions

• Peripheral Arterial Disease

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.