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CERAMENT G Device Registry

Who can join

Ages 18 and older · All sexes

Inclusion Criteria:

* 18 years and over (on the day of surgery)
* receive CERAMENT\|G as a component of their treatment at a participating, contracted centre 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 form.

Exclusion Criteria:

* Any exclusion criteria as per IFU for CERAMENT\|G
* Any off-label use

About the study

This is an Observational Device Registry Study of CERAMENT\|G in normal use in accordance with the IFU. It will run for a period of three years from enrolment of the first patient into the Study at each Site, before being subject to review. A Device Registry is a form of observational study that concerns the performance of a device in normal use. It is intended to collect data that is reflective of 'real world' device performance.

What is being tested

• CERAMENT G (device)

Sponsor: BONESUPPORT AB · Participants: 100 · Started: Aug 17, 2023

Contact the study team

• Brian M Bartholdi · Phone: 16178923927

Official record on ClinicalTrials.gov — NCT06010433

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.