CERAMENT G Device Registry
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBONESUPPORT AB
About this trial
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.
Eligibility criteria
Qualifiers
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.
Disqualifiers
Any exclusion criteria as per IFU for CERAMENT|G
Any off-label use
Trial design
Treatments tested in this trial
- CERAMENT G
Treatment groups
No treatment groups listed
Sponsors and collaborators
Source ClinicalTrials.gov