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Orthofix PhysioStim PEMF Ankle Fusion Retrospective

NCT07282067 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2025-12-29

No results posted yet for this study

Summary

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

Conditions

  • Ankle Fusion
  • Hindfoot Arthrodesis
  • Ankle Arthrodesis
  • Tibiotalar Arthrodesis

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)

Sponsors & Collaborators

  • Orthofix Inc.

    lead INDUSTRY

Eligibility

Min Age
23 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-23
Primary Completion
2026-03-31
Completion
2026-03-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07282067 on ClinicalTrials.gov