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

This study is currently recruiting participants. (see Contacts and Locations)
Verified January 2013 by University Hospital, Ghent
Sponsor:
Information provided by (Responsible Party):
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00284297
First received: January 30, 2006
Last updated: January 29, 2013
Last verified: January 2013

January 30, 2006
January 29, 2013
September 2005
July 2013   (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 ] [ Designated as safety issue: Yes ]
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
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: 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.
 
Recruiting
20
July 2013
July 2013   (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:

-

Both
18 Years and older
No
Contact: René Verdonk, MD, PhD + 32 9 332.22.48 rene.verdonk@ugent.be
Belgium
 
NCT00284297
2005/213
No
University Hospital, Ghent
University Hospital, Ghent
Not Provided
Principal Investigator: René Verdonk, MD, PhD University Hospital, Ghent
University Hospital, Ghent
January 2013

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