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Cytokine Profile and Metal Ion Concentrations at Patients Undergoing a Revision THR
This study is currently recruiting participants.
Verified by Frederiksberg University Hospital, July 2007
First Received: February 9, 2006   Last Updated: July 3, 2007   History of Changes
Sponsored by: Frederiksberg University Hospital
Information provided by: Frederiksberg University Hospital
ClinicalTrials.gov Identifier: NCT00289679
  Purpose

To evaluate the concentration of cytokines and metal ions in blod samples and biopsies from patients undergoing a hip revision.


Condition Intervention Phase
Hip Revision
Device: Hip prosthesis revision
Phase IV

U.S. FDA Resources
Study Type: Interventional
Study Design: Non-Randomized, Open Label, Active Control, Parallel Assignment
  Eligibility

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

Inclusion Criteria: -THR revision

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00289679

Contacts
Contact: arne borgwardt, md 004538163450 arne@borgwardt.com

Locations
Denmark
Frederiksberg University Hospital Recruiting
Frederiksberg, Denmark, 2000
Contact: arne borgwardt, md     004538163450     arne@borgwardt.com    
Sponsors and Collaborators
Frederiksberg University Hospital
Investigators
Principal Investigator: arne borgwardt, md Frederiksberg University Hospital
  More Information

No publications provided

Study ID Numbers: kf 01059/04
Study First Received: February 9, 2006
Last Updated: July 3, 2007
ClinicalTrials.gov Identifier: NCT00289679     History of Changes
Health Authority: Denmark: Ethics Committee

ClinicalTrials.gov processed this record on May 07, 2009