CERAMENT™| Bone Void Filler Device Registry

BONESUPPORT

Status: Enrolling

Conditions: Orthopedic Disorder

Treatments: Device: CERAMENT BVF

Study type: Observational

Funder types: Industry

Identifiers

NCT04244942

S025/2018

Details and patient eligibility

About

A device registry to compile data on the performance of CERAMENT BONE VOID FILLER in normal use.

Full description

A device registry to compile data on the performance of CERAMENT BONE VOID FILLER in normal use.

Enrollment: 300 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 18 years and over (on the day of surgery)
• Receive CERAMENT BVF as a component of their treatment at a participating, contracted center 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

Exclusion criteria

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