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ACTIVE NOT RECRUITING
NCT07282067

Orthofix PhysioStim PEMF Ankle Fusion Retrospective

Sponsor: Orthofix Inc.

View on ClinicalTrials.gov

Summary

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

Official title: A Retrospective Study to Assess the Efficacy of PEMF Treatment in Ankle Fusion

Key Details

Gender

All

Age Range

23 Years - Any

Study Type

OBSERVATIONAL

Enrollment

200

Start Date

2025-01-23

Completion Date

2026-03

Last Updated

2025-12-29

Healthy Volunteers

No

Interventions

DEVICE

Pulsed electromagnetic field (PEMF) stimulation

Subjects treated with PEMF with be directed to use the device for 3 hours per day, up to 6 months or until no longer needed.

OTHER

Control

Control (no PEMF)

Locations (8)

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