CERAMENT™| Bone Void Filler Device Registry

Recruiting now

Conditions studied: Orthopedic Disorder

In brief

A device registry to compile data on the performance of CERAMENT BONE VOID FILLER in normal use.

Key facts

Study ID

NCT04244942

Run by

BONESUPPORT AB

People needed

300

Starts

2020-03-30

Expected to finish

2028-03-30

Last updated by the study team

2025-09-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 years and over (on the day of surgery)
• Receive CERAMENT BVF as a component of their treatment at a participating, contracted center or healthcare provider, in accordance with the IFU for the implanted product
• In receipt of patient information leaflet and have signed appropriately designed informed consent

You may not qualify if…

• Any exclusion criteria as per IFU for CERAMENT BVF
• Any off-label use

Where it is running

• HonorHealth — Scottsdale, Arizona, United States (enrolling)
• Golden Orthopedic Knee, Hip, Shoulder and Foot Center — Boca Raton, Florida, United States (enrolling)
• Sports and Orthopedic Center — Boca Raton, Florida, United States (enrolling)
• Dr. Peter Merkle — Pompano Beach, Florida, United States (enrolling)
• Florida Orthopedic Foot & Ankle Center — Sarasota, Florida, United States (enrolling)
• James Cottom — Sarasota, Florida, United States (enrolling)
• OrthoCarolina — Charlotte, North Carolina, United States (enrolling)
• University Hospitals Cleveland Medical Center — Cleveland, Ohio, United States (enrolling)
• University of Kentucky — Lexington, Kentucky, United States (enrolling)
• Massachusetts General Hospital — Boston, Massachusetts, United States (enrolling)
• The Research Foundation of The State University of New York — Syracuse, New York, United States (enrolling)
• Indiana University — Indianapolis, Indiana, United States
• OrthoIndy — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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