U.S., Dec. 16 -- ClinicalTrials.gov registry received information related to the study (NCT07282067) titled 'Orthofix PhysioStim PEMF Ankle Fusion Retrospective' on Dec. 02.
Brief Summary: This study examines the effect of using the PhysioStim bone growth stimulator on subjects undergoing treatment for ankle and hindfoot fusion surgery.
Study Start Date: Jan. 23
Study Type: OBSERVATIONAL
Condition:
Ankle Fusion
Hindfoot Arthrodesis
Ankle Arthrodesis
Tibiotalar Arthrodesis
Intervention:
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)
Recruitment Status: ACTIVE_NOT_REC...