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Clinical Experience With the Hindfoot Arthrodesis Nail for the Surgical Treatment of Ankle and Hindfoot Pathologies

NCT00942032 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 39

Last updated 2011-04-07

No results posted yet for this study

Summary

The aim of this observational study is to collect and evaluate the current clinical experience gained from the Hindfoot Arthrodesis Nail (HAN) for ankle and hindfoot fusions.

Conditions

  • Hindfoot Arthrodesis
  • Hindfoot Pathologies

Sponsors & Collaborators

  • Synthes Inc.

    collaborator INDUSTRY

  • AO Clinical Investigation and Publishing Documentation

    lead OTHER

Principal Investigators

  • Beate P. Hanson, MD · Ao Clinical Investigation and Documentation, Davos, Switzerland

  • Andrew K. Sands, MD · St. Vincent's Hospital, Foot and Ankle Surgery

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-05-31
Primary Completion
2011-04-30
Completion
2011-04-30

Countries

  • United States
  • France
  • Germany
  • Sweden

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 NCT00942032 on ClinicalTrials.gov