A Pilot Study of Fuzzy Wale Compression Stockinet to Evaluate Healing Following Transtibial Amputation for Peripheral Arterial Disease
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• \>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.
Locations
United States
Minnesota
Mayo Clinic
RECRUITING
Rochester
Contact Information
Primary
Vascular Research Team
Melin.Matthew@mayo.edu
(507) 538-7425
Backup
Matthew Melin, M.D.
Melin.Matthew@mayo.edu
(507) 266-6717
Time Frame
Start Date: 2025-07-07
Estimated Completion Date: 2025-12
Participants
Target number of participants: 40
Treatments
Experimental: Fuzzy Wale Compression Stockinet
Subjects with peripheral arterial disease requiring transtibial amputation will have Fuzzy Wale Compression Stockinet applied and utilized for 4-8 weeks post operatively or until prosthetic fitting and wound has achieved full durable healing.
No_intervention: Standard of care
Subjects with peripheral arterial disease requiring transtibial amputation will receive standard of care treatment compression stockinet.
Related Therapeutic Areas
Sponsors
Leads: Mayo Clinic