Status:
COMPLETED
Clinical Experience With the Hindfoot Arthrodesis Nail for the Surgical Treatment of Ankle and Hindfoot Pathologies
Lead Sponsor:
AO Clinical Investigation and Publishing Documentation
Collaborating Sponsors:
Synthes Inc.
Conditions:
Hindfoot Arthrodesis
Hindfoot Pathologies
Eligibility:
All Genders
Brief 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 m...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- HAN fusion procedure ≥ 12 months before entering the study.
- Written or oral informed consent.
Exclusion
Key Trial Info
Start Date :
May 1 2009
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 1 2011
Estimated Enrollment :
39 Patients enrolled
Trial Details
Trial ID
NCT00942032
Start Date
May 1 2009
End Date
April 1 2011
Last Update
April 7 2011
Active Locations (7)
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1
Eisenhower Medical Center
Rancho Mirage, California, United States, 92270
2
Medical University of South Carolina
Charleston, South Carolina, United States, 29425
3
Harborview Medical Center
Seattle, Washington, United States, 98104-2499
4
Centre Hospitalier Universitaire d'Angers
Angers, France, 49933