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Study identifier: NCT07225751 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Prospective, Randomized, Single-blind, Controlled, Multi-center Study to Assess the Safety and Performance of MagnetOsTM Compared to Autogenous Bone Graft in Patients Undergoing Hindfoot or Ankle Fusions.

Condition: Ankle Arthrodesis or Arthroplasty · Hindfoot Fusion · Ankle Deformity  ·  Sponsor: Kuros Biosurgery AG

PhaseNA
Planned participants126
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This is a phase IV post-marketing study for MagnetOs Putty and MagnetOs Easypack Putty. MagnetOs is a synthetic bone graft extender product that is routinely used by surgeon as treatment for hindfoot and ankle disorders. In this study, MagnetOs Putty and MagnetOs Easypack Putty will be use according to the latest Instructions For Use, standalone in the foot and ankle.

This description comes directly from the study's public registry record.

Talk to the study team

Cesar Silva, MD  ·  9702156793  ·  cesar.silva@kurosbio.com

Always discuss trial participation with your own doctor first.

Locations (6)

Steadman Philippon Research InstituteVail, Colorado, United StatesRecruiting
Hughston Foundation IncColumbus, Georgia, United StatesRecruiting
OrthoCarolina Research Institute, IncCharlotte, North Carolina, United StatesRecruiting
Reconstructive Orthopaedic Associates II dba Rothman Orthopaedic InstitutePhiladelphia, Pennsylvania, United StatesRecruiting
Integrity Orthopedics and Sports MedicineChattanooga, Tennessee, United StatesRecruiting
Centers for Advanced OrthopaedicsFalls Church, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07225751