A Clinical Investigation of ArComXL® Polyethylene in Total Hip Replacement

NCT00698152 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 149

Last updated 2020-03-30

No results posted yet for this study

Summary

The purpose of this data collection is to determine long term survival rate of ArComXL® highly cross-linked polyethylene

Conditions

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Kacy Arnold, MBA · Zimmer Biomet

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-23
Primary Completion
2016-01-15
Completion
2016-01-15

Countries

  • United States

Study Locations

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Entities

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 NCT00698152 on ClinicalTrials.gov