Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Z Revision Femoral Stems

NCT04064008 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2023-11-14

No results posted yet for this study

Summary

Single center, prospective follow-up of previously implanted subjects

Conditions

  • Joint Disease

Interventions

DEVICE

PROFEMUR® Z Revision Femoral Stem

Total Hip Total Hip Arthroscopy

Sponsors & Collaborators

  • MicroPort Orthopedics Inc.

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-04-04
Primary Completion
2030-04-30
Completion
2030-04-30

Countries

  • Poland

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 NCT04064008 on ClinicalTrials.gov