Follow-up of Patients After 4-row Arthrodesis or Proximal Row Carpectomy

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:
NCT00284310
First received: January 30, 2006
Last updated: January 29, 2013
Last verified: January 2013
  Purpose

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.


Condition Intervention
Wrist Surgery
Procedure: Anamnesis and clinical examination

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Follow-up of Patients After 4-row Arthrodesis or Proximal Row Carpectomy

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • Results of both types of wrist surgery [ Time Frame: 5 to 10 years follow up ] [ Designated as safety issue: No ]

Estimated Enrollment: 40
Study Start Date: October 2005
Estimated Study Completion Date: December 2020
Estimated Primary Completion Date: July 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: wrist surgery Procedure: Anamnesis and clinical examination
Anamnesis and clinical examination to follow.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • All patients who underwent wrist surgery (4-row arthrodesis or proximal row carpectomy) between 1998 and 2004
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00284310

Contacts
Contact: Wim Vanhove, MD + 32 9 332.28.31 wim.vanhove@UGent.be

Locations
Belgium
University Hospital Ghent Recruiting
Ghent, Belgium, 9000
Contact: Wim Vanhove, MD    + 32 9 332.28.31    wim.vanhove@UGent.be   
Sponsors and Collaborators
University Hospital, Ghent
Investigators
Principal Investigator: Rene Verdonk, MD, PhD University Hospital, Ghent
  More Information

Additional Information:
No publications provided

Responsible Party: University Hospital, Ghent
ClinicalTrials.gov Identifier: NCT00284310     History of Changes
Other Study ID Numbers: 2005/183
Study First Received: January 30, 2006
Last Updated: January 29, 2013
Health Authority: Belgium: Institutional Review Board

Keywords provided by University Hospital, Ghent:
Wrist surgery: 4-corner arthrodesis or proximal row carpectomy

ClinicalTrials.gov processed this record on September 30, 2014