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

This study is currently recruiting participants.

Verified by University Hospital, Ghent, April 2009

First Received: January 30, 2006 Last Updated: April 7, 2009 History of Changes

Sponsor:	University Hospital, Ghent
Information provided by:	University Hospital, Ghent
ClinicalTrials.gov Identifier:	NCT00284297

Purpose

Follow-up of patients who underwent a knee arthrodesis with different types of intramedullary nails.

Condition	Intervention
Knee Arthrodesis With Intramedullary Nail	Procedure: History taken and clinical examination

Study Type:	Interventional
Study Design:	Treatment, Non-Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study
Official Title:	Follow-up of Patients After Knee Arthrodesis With an Intramedullary Nail

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:

Follow-up of patients who underwent a knee arthrodesis with different types of intramedullary nails [ Designated as safety issue: Yes ]

Estimated Enrollment:	20
Study Start Date:	September 2005
Estimated Study Completion Date:	December 2009
Estimated Primary Completion Date:	December 2009 (Final data collection date for primary outcome measure)

Eligibility

Criteria

Inclusion Criteria:

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

Exclusion Criteria:

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00284297

Contacts

Contact: René Verdonk, MD, PhD

+ 32 9 332.22.48

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:

Website University Hospital Ghent This link exits the ClinicalTrials.gov site

No publications provided

Responsible Party:	University Hospital Ghent ( Rene Verdonk )
Study ID Numbers:	2005/213
Study First Received:	January 30, 2006
Last Updated:	April 7, 2009
ClinicalTrials.gov Identifier:	NCT00284297 History of Changes
Health Authority:	Belgium: Institutional Review Board

Additional relevant MeSH terms:

Musculoskeletal Diseases
Joint Diseases
Ankylosis

ClinicalTrials.gov processed this record on February 08, 2010