- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02045615
Removal Wichita Fusion Nail After Knee Arthrodesis
November 16, 2020 updated by: Universitaire Ziekenhuizen KU Leuven
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.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Pellenberg, Belgium, 3212
- UZ Leuven
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All patients who had to have their Wichita Fusion Nail extracted
Description
Inclusion Criteria:
- Extraction of Wichita Fusion Nail
Exclusion Criteria:
- All other kinds of intramedullairy nails used to become a solid knee arhrodesis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Conventional
Conventional technique for Wichita nail extraction
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New
Proposed technique for Wichita nail extraction
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Operation technique
Time Frame: first 4 months postop
|
Was the arthrodesis site left intact?
How was the Nail removed?
Time for operation?
|
first 4 months postop
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mobility
Time Frame: 1 year postop
|
1 year postop
|
|
|
Pain measurement following the Visual Analogue Scale
Time Frame: 1 year postop
|
1 year postop
|
|
|
Major complications after removal
Time Frame: first 2 years postop
|
Amputation? Infection?
Wound problems?
|
first 2 years postop
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 1, 2013
Primary Completion (Actual)
July 1, 2014
Study Completion (Actual)
July 1, 2014
Study Registration Dates
First Submitted
January 21, 2014
First Submitted That Met QC Criteria
January 23, 2014
First Posted (Estimate)
January 27, 2014
Study Record Updates
Last Update Posted (Actual)
November 18, 2020
Last Update Submitted That Met QC Criteria
November 16, 2020
Last Verified
November 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- S56066
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Removal Wichita Fusion Nail After Knee Arthrodesis
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University Hospital, GhentCompletedKnee Arthrodesis With Intramedullary NailBelgium
-
University of UtahActive, not recruitingPseudarthrosis After Fusion or ArthrodesisUnited States
-
National Taiwan University HospitalUnknownMetal Staple Removal After Total Knee ReplacementTaiwan
Clinical Trials on Proposed technique for removal of the Wichita Fusion Nail
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Thomas Jefferson UniversityCompleted
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Medical University of WarsawCompleted
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Mohamed Tahar Maamouri University HospitalCompletedCongenital Webbing of Neck
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Ambu Inc.Ambu A/SCompletedCystoscopy | Ureteral StentUnited States
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Vita CareJohnson & JohnsonRecruitingKnee Injuries | ACL Injury | Sports Injury | ACL TearBrazil
-
Sequana Medical N.V.CompletedRefractory or Recurrent AscitesSpain, United Kingdom, Italy, France, Austria
-
Sohag UniversityRecruiting
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Vireo Systems, Inc.Princeton Consumer ResearchCompletedBioavailability and AUCUnited States
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CMC Ambroise ParéCompletedIsthmic Spondylolisthesis Treated With Combined Approach: Clinical and Radiological Outcomes (SPLAC)Surgical Procedure, Unspecified | Isthmic SpondylolisthesisFrance