Actively Recruiting
CERAMENT G Device Registry
Led by BONESUPPORT AB · Updated on 2025-09-26
100
Participants Needed
3
Research Sites
266 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
CERAMENT G Device Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years and over (on the day of surgery)
- Receiving CERAMENT|G as part of treatment at a participating healthcare center following the device's instructions for use
- Received patient information leaflet and signed informed consent form
You will not qualify if you...
- Any exclusion criteria specified in the instructions for use for CERAMENT|G
- Any off-label use of CERAMENT|G
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
North Park Podiatry
San Diego, California, United States, 92104
Actively Recruiting
2
OrthoCarolina
Charlotte, North Carolina, United States, 28207
Actively Recruiting
3
University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States, 44106
Actively Recruiting
Research Team
B
Brian M Bartholdi
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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