Bone filler registry launches to monitor safety and healing
NCT ID NCT04244942
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is a registry that collects information on how well the CERAMENT bone void filler works in everyday medical practice. About 300 people receiving the filler during surgery will be followed for up to 18 months. The goal is to track any unexpected device issues, side effects, and how well the bone heals.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2020
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The racial, gender, and ethnic characteristics of the individuals approached for participation in this Observational Registry Study shall reflect the demographics of patients that would ordinarily received CERAMENT BVF for the treatment of their condition at the designated investigative centers. No individuals shall be excluded from participation in the Observational Registry Study based on race, nationality, ethnicity, gender or sexuality.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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 Exclusion Criteria: * Any exclusion criteria as per IFU for CERAMENT BVF * Any off-label use
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
11 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Dr. Peter Merkle
RECRUITINGPompano Beach, Florida, 33064, United States
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Florida Orthopedic Foot & Ankle Center
RECRUITINGSarasota, Florida, 34233, United States
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Golden Orthopedic Knee, Hip, Shoulder and Foot Center
RECRUITINGBoca Raton, Florida, 33434, United States
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HonorHealth
RECRUITINGScottsdale, Arizona, 85258, United States
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Indiana University
TERMINATEDIndianapolis, Indiana, 46202, United States
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James Cottom
RECRUITINGSarasota, Florida, 34233, United States
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Massachusetts General Hospital
RECRUITINGBoston, Massachusetts, 02114, United States
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OrthoCarolina
RECRUITINGCharlotte, North Carolina, 28207, United States
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OrthoIndy
COMPLETEDIndianapolis, Indiana, 46278, United States
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Sports and Orthopedic Center
RECRUITINGBoca Raton, Florida, 33434, United States
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The Research Foundation of The State University of New York
RECRUITINGSyracuse, New York, 13210, United States
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University Hospitals Cleveland Medical Center
RECRUITINGCleveland, Ohio, 44106, United States
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University of Kentucky
RECRUITINGLexington, Kentucky, 40536, United States
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