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Preheating of Femur Component in Hybrid Total Hip Arthroplasty
This study is ongoing, but not recruiting participants.
First Received: April 27, 2006   Last Updated: December 3, 2007   History of Changes
Sponsored by: Northern Orthopaedic Division, Denmark
Information provided by: Northern Orthopaedic Division, Denmark
ClinicalTrials.gov Identifier: NCT00319085
  Purpose

Background

  • Recently published studies confirm that preheating of femoral component enhances shear strength of implant-cement interface. Both Iesaka et al 2003 and Jafri et al 2004 showed reduction in cement porosity on cement-implant interface with preheated femur components. We will use the radiostereometry analysis (RSA) to investigate how the preheating of femur component influence on prosthesis survivorship. There are no clinical controlled studies performed to the date.

The aim of the study

  • Comparison of the migration rates between preheated and non-preheated femur components, analyzed with RSA.

Methods

  • We will randomize 80 patients into 2 groups with 40 in each. All the patients will undergo standard hybrid total hip replacement. In group one the femur component (Bi-Metric, Interlock Biomet) will be preheated to 40 degrees of Celsius before cementation. In group two- also control group- the femur component will be of room temperature. We will measure the temperature at cement bone interface during the operation with use of thermocouple electrodes inserted through separate drill hole in the femur. The measurements will be recorded every 10 seconds. The patients will follow the standard postoperative rehabilitation program.
  • The RSA analysis will be performed the first day after the operation and at 3, 12, 24 months postoperatively.
  • The Dual-energy X-ray absorptiometry scanning (DEXA) of the femur will be performed at the first week after the operation and at 12 and 24 months postoperatively.
  • The patients will be followed both clinically and radiological at 1 and 2 years after the operation (Harris Hip Score).
  • The results will be expressed as mean + SD (in mm). ANOVA statistical analysis will be used to confirm the differences between the groups.

Condition Intervention
Osteoarthritis, Hip
Procedure: Total hip replacement (Preheating of femur stem)

MedlinePlus related topics: Osteoarthritis Surgery
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Single Group Assignment, Efficacy Study
Official Title: Comparison Between Preheated and Non-Preheated Femur Component in Hybrid Total Hip Arthroplasty (THA) A Prospective Randomized Study of the 80 THA Using Radiostereometry.

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

Primary Outcome Measures:
  • Stem migration in mm

Secondary Outcome Measures:
  • Bone mineral density g/cm2
  • Temperature at bone-cement interface, degrees in Celsius
  • Serum- Titanium measurements in blood samples

Estimated Enrollment: 80
Study Start Date: May 2006
Estimated Study Completion Date: December 2010
  Eligibility

Ages Eligible for Study:   70 Years to 85 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • The patients suffering of hip osteoarthritis

Exclusion Criteria:

  • The patients with ASA score >II
  • The patients with cancer
  • The secondary coxarthrosis after the trauma
  • Any vascular or neuromuscular diseases affecting the hip.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00319085

Locations
Denmark
Farsoe Hospital, Northern Orthopaedic Division
Farsoe, Denmark, 9640
Sponsors and Collaborators
Northern Orthopaedic Division, Denmark
Investigators
Principal Investigator: Mogens B Jørgensen, dr. Northern Orthopaedic Division
Principal Investigator: Mogens B Laursen, Ph.D Northern Orthopaedic Division
Principal Investigator: Lotte Borgwardt, dr. Frederikberg Hospital, Copenhagen
Study Chair: Kjeld Søballe, Ph.D., MD. University Hospital of Aarhus
Study Director: Poul T Nielsen, dr. Northern Orthopaedic Division
  More Information

No publications provided

Study ID Numbers: ON-04-008a-JPE
Study First Received: April 27, 2006
Last Updated: December 3, 2007
ClinicalTrials.gov Identifier: NCT00319085     History of Changes
Health Authority: Denmark: National Board of Health

Keywords provided by Northern Orthopaedic Division, Denmark:
Arthroplasty,
Hip,
Pre-heating,
Radiostereometric analysis,
Dual-Energy Radiographic Absorptiometry,

Study placed in the following topic categories:
Musculoskeletal Diseases
Osteoarthritis
Joint Diseases
Arthritis
Rheumatic Diseases
Osteoarthritis, Hip

Additional relevant MeSH terms:
Musculoskeletal Diseases
Osteoarthritis
Joint Diseases
Arthritis
Rheumatic Diseases
Osteoarthritis, Hip

ClinicalTrials.gov processed this record on May 06, 2009