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Clinical Study of Bone Graft Substitutes in Orthopaedic and Spinal Applications.

NCT03570606 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 220

Last updated 2025-04-04

No results posted yet for this study

Summary

This is an observational, prospective, non-randomised, multi-centred post market clinical follow-up study to compile real world clinical data on safety and efficacy of the synthetic bone graft substitutes in a commercial clinical setting in long bone and extremity defects and in spinal fusion procedures.

Conditions

  • Bone Deformity

Interventions

DEVICE

bone graft substitute

orthopaedic or spine bony defects

Sponsors & Collaborators

  • Ceramisys Ltd

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-13
Primary Completion
2026-03-31
Completion
2026-06-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03570606 on ClinicalTrials.gov