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Retrospective Collection of Safety and Performance Data

NCT04644536 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2024-11-07

No results posted yet for this study

Summary

This is a retrospective 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 Defects

Interventions

DEVICE

Bone graft substitute

Orthopaedic or Spine bony defects

Sponsors & Collaborators

  • Bioceramed

    lead INDUSTRY

Principal Investigators

  • Nuno A Ribeiro, MD · Hospital Lusíadas Lisboa

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-11-25
Primary Completion
2024-11-06
Completion
2024-11-06

Countries

  • Portugal

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 NCT04644536 on ClinicalTrials.gov