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Follow-up of Patients After 4-Row Arthrodesis or Proximal Row Carpectomy
This study is currently recruiting participants.
Study NCT00284310   Information provided by University Hospital, Ghent
First Received: January 30, 2006   Last Updated: April 7, 2009   History of Changes

January 30, 2006
April 7, 2009
October 2005
December 2009   (final data collection date for primary outcome measure)
Results of both types of wrist surgery [ Designated as safety issue: No ]
Results of both types of wrist surgery
Complete list of historical versions of study NCT00284310 on ClinicalTrials.gov Archive Site
 
 
 
Follow-up of Patients After 4-Row Arthrodesis or Proximal Row Carpectomy
Follow-up of Patients After 4-Row Arthrodesis or Proximal Row Carpectomy

The purpose of this trial is to follow-up on patients who underwent different types of wrist surgery: 4-row arthrodesis or proximal row carpectomy.

 
 
Interventional
Treatment, Non-Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study
Wrist Surgery
Procedure: Anamnesis and clinical examination
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
40
December 2009
December 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • All patients who underwent wrist surgery (4-row arthrodesis or proximal row carpectomy) between 1998 and 2004
Both
18 Years and older
No
Contact: Wim Vanhove, MD + 32 9 332.28.31 wim.vanhove@UGent.be
Belgium
 
NCT00284310
Wim Vanhove, University Hospital Ghent
2005/183
University Hospital, Ghent
 
Principal Investigator: Rene Verdonk, MD, PhD University Hospital, Ghent
University Hospital, Ghent
April 2009

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