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

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ClinicalTrials.gov Identifier: NCT00284297
Recruitment Status : Unknown
Verified December 2014 by University Hospital, Ghent.
Recruitment status was:  Recruiting
First Posted : January 31, 2006
Last Update Posted : December 5, 2014
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
Follow-up of patients who underwent a knee arthrodesis with different types of intramedullary nails.

Condition or disease Intervention/treatment
Knee Arthrodesis With Intramedullary Nail Procedure: History taken and clinical examination

Study Design

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 20 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Follow-up of Patients After Knee Arthrodesis With an Intramedullary Nail
Study Start Date : September 2005
Estimated Primary Completion Date : July 2015
Estimated Study Completion Date : July 2015
Arms and Interventions

Arm Intervention/treatment
Experimental: knee arthrodesis Procedure: History taken and clinical examination
History is taken and clinical examination is followed


Outcome Measures

Primary Outcome Measures :
  1. Follow-up of patients who underwent a knee arthrodesis with different types of intramedullary nails [ Time Frame: t0 ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

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

Exclusion Criteria:

Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00284297


Contacts
Contact: René Verdonk, MD, PhD + 32 9 332.22.48 rene.verdonk@ugent.be

Locations
Belgium
University Hospital Ghent Recruiting
Ghent, Belgium, 9000
Contact: René Verdonk, MD, PhD    + 32 9 332.22.48    rene.verdonk@ugent.be   
Principal Investigator: René Verdonk, MD, PhD         
Sponsors and Collaborators
University Hospital, Ghent
Investigators
Principal Investigator: René Verdonk, MD, PhD University Hospital, Ghent
More Information

Additional Information:
Responsible Party: University Hospital, Ghent
ClinicalTrials.gov Identifier: NCT00284297     History of Changes
Other Study ID Numbers: 2005/213
First Posted: January 31, 2006    Key Record Dates
Last Update Posted: December 5, 2014
Last Verified: December 2014