Study Comparing Marathon Polyethylene and Enduron Polyethylene Acetabular Liners Used in Total Hip Arthroplasty
Primary Purpose
Osteoarthritis, Arthritis, Joint Diseases
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Total Hip Replacement
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis focused on measuring Osteolysis, Polyethylene, Crosslinked Polyethylene, Total Hip Replacement, CT
Eligibility Criteria
Inclusion Criteria:
(from original study)
-Elective total hip replacement patient
(from 10-year follow-up)
- Consented to the original study.
- Received a Duraloc 100 cup with either a crosslinked Marathon or standard Enduron liner.
- Received an AML/Solution or a Prodigy stem with 28mm cobalt chrome femoral head.
Exclusion Criteria:
(from original study)
-None
(from 10-year follow-up)
- Patient did not receive device as specified in inclusion criteria.
- Patient refused to consent to the 10-year follow-up.
Sites / Locations
- Anderson Orthopaedic Research Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Crosslinked Marathon polyethylene
Standard Enduron polyethylene
Arm Description
Outcomes
Primary Outcome Measures
Incidence of Clinically Significant Osteolysis
The incidence of clinically significant osteolysis was based on the number of unrevised THAs (total hip arthroplasties) with at least 1.5 square centimeters of pelvic and/or femoral osteolysis. Osteolysis was defined as an area of localized loss of trabecular bone or cortical erosion that was not apparent on the pre-operative or immediate postoperative radiograph. To obtain lesion sizes, the defects were outlined on the anteroposterior pelvic radiograph and the area of the lesion was measured using Martell's Hip Analysis Suite software. Lesions were considered clinically important if the total area of osteolysis around a hip replacement was at least 1.5 square centimeters.
Secondary Outcome Measures
Polyethylene Wear
A single reviewer, who was blinded to the type of polyethylene liner, evaluated femoral head penetration among all unrevised hips with minimum 9-year radiographic follow-up using serial anteroposterior pelvic radiographs. Two-dimensional head penetration was determined for each follow-up radiograph relative to the immediate post-operative (nominal 6-week follow-up) reference view using Hip Suite Analysis version 8.0 with elliptical correction, a validated, computer-assisted technique. A linear wear rate was evaluated for each hip that had a minimum of three follow-up radiographs by using a least-squares linear regression to calculate the slope of the best-fit line for the wear vector magnitude versus time in situ data. The slope from this regression represented the steady-state linear wear rate. The steady-state linear wear rate data from all hips in a group was used to compute a mean polyethylene wear value.
Rate of Reoperation
The rate of reoperation was based on the number of reoperations in each group. Any additional surgery after a participant's initial hip replacement was considered a reoperation.
Harris Hip Score
The Harris Hip Score measures outcome after hip replacement and is based on a scale from 0 (worst) to 100 (best).
Patient Satisfaction
Patient satisfaction was quantified by asking participants to respond "yes" or "no" to the question, "Are you satisfied with the results of your hip operation?"
Full Information
NCT ID
NCT01121146
First Posted
May 10, 2010
Last Updated
November 3, 2014
Sponsor
Anderson Orthopaedic Research Institute
Collaborators
DePuy Orthopaedics
1. Study Identification
Unique Protocol Identification Number
NCT01121146
Brief Title
Study Comparing Marathon Polyethylene and Enduron Polyethylene Acetabular Liners Used in Total Hip Arthroplasty
Official Title
A Prospective, Randomized Clinical Study Comparing Marathon Polyethylene and Enduron Polyethylene Acetabular Liners Used in Total Hip Arthroplasty
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
December 1998 (undefined)
Primary Completion Date
March 2012 (Actual)
Study Completion Date
March 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Anderson Orthopaedic Research Institute
Collaborators
DePuy Orthopaedics
4. Oversight
5. Study Description
Brief Summary
The purpose of the study is to determine whether crosslinked Marathon and standard Enduron polyethylene liners show differences in bone loss around the hip implant.
Detailed Description
Several institutions report very low wear rates with highly crosslinked polyethylene based on early clinical data. However, since bone loss typically appears after 5-year follow-up, the reduction in the incidence and extent of bone loss among total hip replacement patients with crosslinked Marathon liners, compared to those with standard Enduron liners, has not been as dramatic as the wear reduction. Despite the substantial reduction in wear that we observed at 5-year follow-up, the patients' perceptions of their outcomes remained similar among the Marathon and Enduron groups. This study will evaluate outcome at a minimum of 10-years after surgery among the same group of patients whose outcome was previously reported at 5-year follow-up. At 10-year follow-up, we anticipate that the reduction in wear associated with Marathon polyethylene will be associated with significant reductions in bone loss when compared to the Enduron polyethylene.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Arthritis, Joint Diseases, Musculoskeletal Diseases, Rheumatic Diseases
Keywords
Osteolysis, Polyethylene, Crosslinked Polyethylene, Total Hip Replacement, CT
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
236 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Crosslinked Marathon polyethylene
Arm Type
Active Comparator
Arm Title
Standard Enduron polyethylene
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
Total Hip Replacement
Intervention Description
Comparison of Marathon and Enduron polyethylene
Primary Outcome Measure Information:
Title
Incidence of Clinically Significant Osteolysis
Description
The incidence of clinically significant osteolysis was based on the number of unrevised THAs (total hip arthroplasties) with at least 1.5 square centimeters of pelvic and/or femoral osteolysis. Osteolysis was defined as an area of localized loss of trabecular bone or cortical erosion that was not apparent on the pre-operative or immediate postoperative radiograph. To obtain lesion sizes, the defects were outlined on the anteroposterior pelvic radiograph and the area of the lesion was measured using Martell's Hip Analysis Suite software. Lesions were considered clinically important if the total area of osteolysis around a hip replacement was at least 1.5 square centimeters.
Time Frame
Minimum 9-year radiographic follow-up
Secondary Outcome Measure Information:
Title
Polyethylene Wear
Description
A single reviewer, who was blinded to the type of polyethylene liner, evaluated femoral head penetration among all unrevised hips with minimum 9-year radiographic follow-up using serial anteroposterior pelvic radiographs. Two-dimensional head penetration was determined for each follow-up radiograph relative to the immediate post-operative (nominal 6-week follow-up) reference view using Hip Suite Analysis version 8.0 with elliptical correction, a validated, computer-assisted technique. A linear wear rate was evaluated for each hip that had a minimum of three follow-up radiographs by using a least-squares linear regression to calculate the slope of the best-fit line for the wear vector magnitude versus time in situ data. The slope from this regression represented the steady-state linear wear rate. The steady-state linear wear rate data from all hips in a group was used to compute a mean polyethylene wear value.
Time Frame
Minimum 9-year radiographic follow-up
Title
Rate of Reoperation
Description
The rate of reoperation was based on the number of reoperations in each group. Any additional surgery after a participant's initial hip replacement was considered a reoperation.
Time Frame
10-year follow-up
Title
Harris Hip Score
Description
The Harris Hip Score measures outcome after hip replacement and is based on a scale from 0 (worst) to 100 (best).
Time Frame
Minimum 9-year follow-up
Title
Patient Satisfaction
Description
Patient satisfaction was quantified by asking participants to respond "yes" or "no" to the question, "Are you satisfied with the results of your hip operation?"
Time Frame
Minimum 9-year follow-up
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
(from original study)
-Elective total hip replacement patient
(from 10-year follow-up)
Consented to the original study.
Received a Duraloc 100 cup with either a crosslinked Marathon or standard Enduron liner.
Received an AML/Solution or a Prodigy stem with 28mm cobalt chrome femoral head.
Exclusion Criteria:
(from original study)
-None
(from 10-year follow-up)
Patient did not receive device as specified in inclusion criteria.
Patient refused to consent to the 10-year follow-up.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles A. Engh, Sr., MD
Organizational Affiliation
Anderson Orthopaedic Research Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
C. Anderson Engh, Jr., MD
Organizational Affiliation
Anderson Orthopaedic Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Anderson Orthopaedic Research Institute
City
Alexandria
State/Province
Virginia
ZIP/Postal Code
22306
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
17823032
Citation
Leung SB, Egawa H, Stepniewski A, Beykirch S, Engh CA Jr, Engh CA Sr. Incidence and volume of pelvic osteolysis at early follow-up with highly cross-linked and noncross-linked polyethylene. J Arthroplasty. 2007 Sep;22(6 Suppl 2):134-9. doi: 10.1016/j.arth.2007.04.006. Epub 2007 Jul 27.
Results Reference
result
PubMed Identifier
16950057
Citation
Engh CA Jr, Stepniewski AS, Ginn SD, Beykirch SE, Sychterz-Terefenko CJ, Hopper RH Jr, Engh CA. A randomized prospective evaluation of outcomes after total hip arthroplasty using cross-linked marathon and non-cross-linked Enduron polyethylene liners. J Arthroplasty. 2006 Sep;21(6 Suppl 2):17-25. doi: 10.1016/j.arth.2006.05.002.
Results Reference
result
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Study Comparing Marathon Polyethylene and Enduron Polyethylene Acetabular Liners Used in Total Hip Arthroplasty
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