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Cytokine Profile and Metal Ion Concentrations at Patients Undergoing a Revision THR

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified July 2007 by Frederiksberg University Hospital.
Recruitment status was:  Recruiting
Sponsor:
Information provided by:
Frederiksberg University Hospital
ClinicalTrials.gov Identifier:
NCT00289679
First received: February 9, 2006
Last updated: March 17, 2015
Last verified: July 2007
  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 4

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: Open Label

Further study details as provided by Frederiksberg University Hospital:

  Eligibility

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • THR revision
  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: 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

ClinicalTrials.gov Identifier: NCT00289679     History of Changes
Other Study ID Numbers: kf 01059/04
Study First Received: February 9, 2006
Last Updated: March 17, 2015

ClinicalTrials.gov processed this record on June 26, 2017