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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02045615
Other study ID # S56066
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2013
Est. completion date July 2014

Study information

Verified date November 2020
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to make clear how difficult it is to remove osteosynthesis materials afterwards, so surgeons will think twice before inserting intramedullary nails. Also it offers an alternative methode to remove the Wichita Fusion Nail after arthrodesis has become.


Recruitment information / eligibility

Status Completed
Enrollment 4
Est. completion date July 2014
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria: - Extraction of Wichita Fusion Nail Exclusion Criteria: - All other kinds of intramedullairy nails used to become a solid knee arhrodesis

Study Design


Related Conditions & MeSH terms

  • Removal Wichita Fusion Nail After Knee Arthrodesis

Intervention

Procedure:
Proposed technique for removal of the Wichita Fusion Nail


Locations

Country Name City State
Belgium UZ Leuven Pellenberg

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Operation technique Was the arthrodesis site left intact? How was the Nail removed? Time for operation? first 4 months postop
Secondary Mobility 1 year postop
Secondary Pain measurement following the Visual Analogue Scale 1 year postop
Secondary Major complications after removal Amputation? Infection? Wound problems? first 2 years postop