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Follow-up of Patients After Knee Arthrodesis With an Intramedullary Nail

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified December 2014 by University Hospital, Ghent.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00284297
First Posted: January 31, 2006
Last Update Posted: December 5, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University Hospital, Ghent
January 30, 2006
January 31, 2006
December 5, 2014
September 2005
July 2015   (Final data collection date for primary outcome measure)
Follow-up of patients who underwent a knee arthrodesis with different types of intramedullary nails [ Time Frame: t0 ]
Follow-up of patients with knee arthrodese with a different type of intramedular nail
Complete list of historical versions of study NCT00284297 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Follow-up of Patients After Knee Arthrodesis With an Intramedullary Nail
Follow-up of Patients After Knee Arthrodesis With an Intramedullary Nail
Follow-up of patients who underwent a knee arthrodesis with different types of intramedullary nails.
Not Provided
Interventional
Not Provided
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Knee Arthrodesis With Intramedullary Nail
Procedure: History taken and clinical examination
History is taken and clinical examination is followed
Experimental: knee arthrodesis
Intervention: Procedure: History taken and clinical examination
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
20
July 2015
July 2015   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • All patients who underwent a knee arthrodesis with an intramedullary nail between 1994 and 2005

Exclusion Criteria:

Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Belgium
 
 
NCT00284297
2005/213
No
Not Provided
Not Provided
University Hospital, Ghent
University Hospital, Ghent
Not Provided
Principal Investigator: René Verdonk, MD, PhD University Hospital, Ghent
University Hospital, Ghent
December 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP