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CERAMENT G Device Registry
NCT06010433 · View on ClinicalTrials.gov ↗
Study 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.
Conditions Studied
Interventions
- DEVICE CERAMENT G
Study Locations (3)
California
- North Park Podiatry — San Diego
North Carolina
- OrthoCarolina — Charlotte
Ohio
- University Hospitals Cleveland Medical Center — Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2023-08-17 |
| Est. Completion | 2028-09-22 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06010433
The ClinicalTrials.gov registry entry for NCT06010433 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BONESUPPORT AB, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Diabetic Foot Osteomyelitis appearing as the primary indexed condition, and to 1 intervention — of which CERAMENT G is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06010433 reports 3 study locations spanning 3 distinct geographic areas — top geographies include California, North Carolina, Ohio. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06010433 about?
NCT06010433 is a clinical study titled "CERAMENT G Device Registry". 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 con...
What is the current status of trial NCT06010433?
This trial is currently recruiting. The enrollment target is 100 participants. The study started on 2023-08-17. Estimated completion is 2028-09-22.
What conditions does trial NCT06010433 study?
This clinical trial studies the following conditions: Diabetic Foot Osteomyelitis, Chronic Osteomyelitis, Fracture Related Infection. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06010433?
The interventions under investigation include: CERAMENT G (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06010433?
This trial is sponsored by BONESUPPORT AB, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06010433 being conducted?
This trial has 3 study locations across California, North Carolina, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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