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Clinical Trials/NCT01289834
NCT01289834
Completed
N/A

A Migration (RSA) and Bone Density (DEXA) Study Comparing Hi-Fatigue Bone Cement and Palacos Bone Cement in Fixation of a Smooth vs. a Fine-blasted Femoral Stem. A Prospective Randomized Study on Primary Total Hip Arthroplasty.

University of Aarhus1 site in 1 country52 target enrollmentAugust 2010
ConditionsHip Arthritis

Overview

Phase
N/A
Intervention
Not specified
Conditions
Hip Arthritis
Sponsor
University of Aarhus
Enrollment
52
Locations
1
Primary Endpoint
Femoral component migration (roentgen stereo photogrammetric analysis - RSA)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this scientific study is to compare early migration of hip prostheses in respect to the bone in order to determine whether there is a clinical difference between the two investigated bone cements (which one is best suited for cementation of hip prostheses).

Detailed Description

A randomized controlled clinical trial on 50 hybrid hips age above 70 years to the described two surgical procedures will be performed at Aarhus University hospital by two orthopaedic consultants. Randomization in 10 blocks of ten patients distributed with five patients for Palacos Cement and five patients for Hi-Fatigue Cement. * 25 CPT femoral stems fixed with Hi-Fatigue Bone Cement. * 25 CPT femoral stems fixed with Palacos Bone Cement. All patients will be operated by the postero-lateral approach. The post-operative treatment and training will not differ from the standard.

Registry
clinicaltrials.gov
Start Date
August 2010
End Date
January 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • primary hip osteoarthritis
  • sufficient bone quality for total hip arthroplasty
  • age 71 years and above
  • no upper age limit if the patient is capable
  • informed and written consent
  • patient can only enter the project with one hip

Exclusion Criteria

  • planned bilateral hip surgery
  • neuromuscular or vascular disease in the affected leg
  • preoperatively not found suitable for a hip arthroplasty
  • patients with osteoporosis based on former diagnosis or preoperative DEXA-scan
  • fracture sequelae, osteonecrosis or previous extensive hip surgery
  • patients who cannot refrain from taking NSAID post-operatively
  • continuous medical treatment with vitamin K antagonists (Warfarin) which is known to reduce the bone mass by a factor of 5
  • patients with metabolic bone disease
  • patients with rheumatoid arthritis
  • postmenopausal women in systemic estrogenic hormone substitution

Outcomes

Primary Outcomes

Femoral component migration (roentgen stereo photogrammetric analysis - RSA)

Time Frame: 2 years

Migration of the femoral component is measured over time and in respect to the femur bone.

Study Sites (1)

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