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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06010433
Study type Observational [Patient Registry]
Source BONESUPPORT AB
Contact Brian M Bartholdi
Phone 16178923927
Email brian.bartholdi@bonesupport.com
Status Not yet recruiting
Phase
Start date September 22, 2023
Completion date September 22, 2028

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