Prevision® PMCF Study

NCT03510065 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2018-04-30

No results posted yet for this study

Summary

Monocentric, non-interventional Post-Market Clinical Follow-Up (PMCF) Study on past implantations of the Prevision® prosthesis; the survival rate of the Prevision® prosthesis shall be evaluated and compared to literature results on comparable Revision stems.

Conditions

  • Survival, Prosthesis

Interventions

DEVICE

Prevision®

One time Evaluation with documentation of one follow-up visit

Sponsors & Collaborators

  • Aesculap AG

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-01
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • Germany

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 NCT03510065 on ClinicalTrials.gov