Clinical Trials Directory

Trials / Completed

CompletedNCT00942032

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

Clinical Experience With the Hindfoot Arthrodesis Nail (HAN) for the Surgical Treatment of Ankle and Hindfoot Pathologies. A Retrospective Case Series.

Status
Completed
Phase
Study type
Observational
Enrollment
39 (actual)
Sponsor
AO Clinical Investigation and Publishing Documentation · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

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.

Detailed description

The HAN (Synthes) is a newly designed, titanium nail for trans-calcaneal, retrograde hindfoot fusion. The lateral bend allows an entry site in the center of the lateral column of the calcaneus, thus minimizing the risk of iatrogenic injury of the plantar neurovascular bundle.

Conditions

Timeline

Start date
2009-05-01
Primary completion
2011-04-01
Completion
2011-04-01
First posted
2009-07-20
Last updated
2011-04-07

Locations

7 sites across 4 countries: United States, France, Germany, Sweden

Source: ClinicalTrials.gov record NCT00942032. Inclusion in this directory is not an endorsement.