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Bimetric-10: Investigation of Patients Who Have Underwent Total Hip Arthroplasty With a Cemented Bi-Metric Stem

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00192699
First Posted: September 19, 2005
Last Update Posted: March 31, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Northern Orthopaedic Division, Denmark
  Purpose
This is a 10 year follow-up investigation of patients who have underwent total hip arthroplasty with a cemented Bimetric stem.

Condition Intervention
Osteoarthrosis Device: Bimetric femoral stem

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: 10 Year Follow-up Investigation of Patients Who Have Underwent Total Hip Arthroplasty With a Cemented Bi-metric Stem

Resource links provided by NLM:


Further study details as provided by Northern Orthopaedic Division, Denmark:

Enrollment: 80
Study Start Date: January 2004
Study Completion Date: April 2011
Primary Completion Date: April 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Group 1: Cemented Bi-Metric femoral stem
Cemented Bi-Metric femoral stem
Device: Bimetric femoral stem
Cemented Bi-Metric femoral stem
Other Name: Cemented Bi-Metric femoral stem

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with osteoarthrosis in hip who have underwent surgery for 10 years ago using Cemented Bi-Metric femoral stem.
Criteria

Inclusion criteria:

  • Osteoarthrosis

Exclusion criteria:

  • Malignancies
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00192699


Locations
Denmark
Northern Orthopaedic Division, Aalborg University Hospital
Aalborg, Northern Jutland, Denmark, 9000
Sponsors and Collaborators
Northern Orthopaedic Division, Denmark
Investigators
Principal Investigator: Mogens B Laursen, MD, PhD Northern Orthopaedic Division, Aalborg University Hospital, Denmark
  More Information

Responsible Party: Northern Orthopaedic Division, Denmark
ClinicalTrials.gov Identifier: NCT00192699     History of Changes
Other Study ID Numbers: ON-04-008b-JPE
First Submitted: September 11, 2005
First Posted: September 19, 2005
Last Update Posted: March 31, 2014
Last Verified: March 2014

Keywords provided by Northern Orthopaedic Division, Denmark:
Osteoarthritis

Additional relevant MeSH terms:
Osteoarthritis
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Metronidazole
Anti-Infective Agents
Antiprotozoal Agents
Antiparasitic Agents