Subchondroplasty Procedure in Patients With Bone Marrow Lesions

NCT03430219 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 93

Last updated 2023-06-22

No results posted yet for this study

Summary

This is a prospective, multi-center, post-market data collection study intended to collect data on the short- and long-term safety and performance of the SCP Procedure.

Conditions

  • Bone Marrow Lesions
  • Bone Marrow Edema

Interventions

DEVICE

Subchondroplasty Procedure

AccuFill is an injectable, self-setting, macro-porous, osteoconductive, calcium phosphate bone graft substitute material that is intended for use to fill bony voids or gaps of the lower extremities (pelvis through foot) that are not intrinsic to the stability of the bony structure

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Peter Angele, Prof.Dr.med · University of Regensburg

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-01
Primary Completion
2023-03-16
Completion
2023-03-16

Countries

  • Germany
  • Italy
  • Netherlands
  • Spain
  • United Kingdom

Study Locations

More Related Trials

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 NCT03430219 on ClinicalTrials.gov