CERAMENT™| Bone Void Filler Device Registry

Purpose

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

Condition

  • Orthopedic Disorder

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

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

Study Design

Phase
Study Type
Observational [Patient Registry]
Observational Model
Case-Only
Time Perspective
Prospective

Recruiting Locations

UK Center for Clinical and Translational Science and nearby locations

University of Kentucky
Lexington, Kentucky 40536
Contact:
Stephen Duncan, MD
stdunc2@uky.edu

More Details

NCT ID
NCT04244942
Status
Recruiting
Sponsor
BONESUPPORT AB

Study Contact

Brian M Bartholdi
6178923927
brian.bartholdi@bonesupport.com

Detailed Description

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