Orthofix PhysioStim PEMF Ankle Fusion Retrospective

Running, not enrolling

Conditions studied: Ankle Fusion, Hindfoot Arthrodesis, Ankle Arthrodesis, Tibiotalar Arthrodesis

In brief

This study examines the effect of using the PhysioStim bone growth stimulator on subjects undergoing treatment for ankle and hindfoot fusion surgery.

Key facts

Study ID

NCT07282067

Run by

Orthofix Inc.

People needed

200

Starts

2025-01-23

Expected to finish

2026-06-30

Last updated by the study team

2026-06-04

Who can join

Age: 23 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Condition requiring ankle fusion surgery or nonoperative treatment for failed ankle fusion
• Age 23 years or older
• Subjects must have a minimum of 6 months follow-up data or evidence of fusion, whichever occurs first

You may not qualify if…

• Subject is a prisoner

Where it is running

• Arizona Foot Health — Phoenix, Arizona, United States
• Phoenix Foot and Ankle Institute — Scottsdale, Arizona, United States
• OrthoArizona — Scottsdale, Arizona, United States
• Byron COllier DPM, Inc — Pismo Beach, California, United States
• East Village Foot and Ankle — Des Moines, Iowa, United States
• Precision Orthopedics and Sports Medicine — Laurel, Maryland, United States
• OrthoCarolina Research Institute, Inc — Charlotte, North Carolina, United States
• Lone Star Orthopaedic and Spine Specialists — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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