CompletedNot Applicable

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

United States, France, Germany39 participantsStarted 2009-05

Plain-language 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.

Who can participate

SexALL

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Inclusion Criteria: * HAN fusion procedure ≥ 12 months before entering the study. * Written or oral informed consent.

What they're measuring

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.

Timeframe: More than 1 year

Trial details

NCT IDNCT00942032

SponsorAO Clinical Investigation and Publishing Documentation

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2011-04

View on ClinicalTrials.gov More Hindfoot Arthrodesis trials