Condition: Chronic Osteomyelitis · Fracture Related Infection · Diabetic Foot Osteomyelitis · Sponsor: BONESUPPORT AB
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.
This description comes directly from the study's public registry record.
Brian M Bartholdi · 16178923927 · brian.bartholdi@bonesupport.com
Always discuss trial participation with your own doctor first.
| North Park Podiatry | San Diego, California, United States | Recruiting |
| OrthoCarolina | Charlotte, North Carolina, United States | Recruiting |
| University Hospitals Cleveland Medical Center | Cleveland, Ohio, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06010433