CERAMENT™| Bone Void Filler Device Registry
Janos Ertl
Primary Investigator
Overview
A device registry to compile data on the performance of CERAMENT BONE VOID FILLER in normal use.
Description
A device registry to compile data on the performance of CERAMENT BONE VOID FILLER in normal use.
Eligibility
You may be eligible for this study if you meet the following criteria:
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Conditions:
Orthopedic Disorder
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Age: 18 Years
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Gender: All
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
Connect with a study center near you
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What happens next?
- You can expect the study team to contact you via email or phone in the next few days.
- Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.
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