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CERAMENT G Device Registry

CERAMENT G Device Registry

Recruiting
18 years and older
All
Phase N/A
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  • Simplified (AI rewritten)

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Overview

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

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • Any exclusion criteria as per IFU for CERAMENT|G
  • Any off-label use

Study details
    Chronic Osteomyelitis
    Fracture Related Infection
    Diabetic Foot Osteomyelitis

NCT06010433

BONESUPPORT AB

15 October 2025

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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