RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hip Stem
Primary Purpose
Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
uncemented total hip arthroplasty
Sponsored by
About this trial
This is an interventional treatment trial for Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis focused on measuring uncemented hip, bone remodeling, DEXA, clinical evaluation
Eligibility Criteria
Inclusion Criteria:Male or non pregnant female patients >18 years
- Patient with degenerative or traumatic changes to hip requiring hip replacement
- Patient with BMI<35
- Patient signed informed consent
Exclusion Criteria:
- chronic anti-inflammatory medication use> 3 months
- revision surgery to the affected femur
- Cancer therapy including immunosuppression, chemotherapy and radiation
- Pathological fractures, delayed ossification or non-union is likely to occur
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
HA-Omnifit
Symax hip stem
Arm Description
Patients who receive a HA-Omnifit uncemented hip stem
Patients with the Symax uncemented hip stem
Outcomes
Primary Outcome Measures
short term bone remodeling
Bone remodeling is determined by measuring the Bone mineral density during time
complications and reoperations
Reporting all complications and reoperations of the two different hip prostheses
Secondary Outcome Measures
clinical performance
Comparison of the clinical performance of the two different hip prostheses
Radiological evaluation
Evaluation of Xrays according to the engh classifications
Full Information
NCT ID
NCT01695213
First Posted
September 25, 2012
Last Updated
September 25, 2012
Sponsor
Maastricht University Medical Center
Collaborators
Stryker European Operations BV
1. Study Identification
Unique Protocol Identification Number
NCT01695213
Brief Title
RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hip Stem
Official Title
A Randomized Comparative Study to Evaluate the Performance and Confirm the Safety of the Diocom Hip Syhstem in Cementless Hip Arthroplasty
Study Type
Interventional
2. Study Status
Record Verification Date
September 2012
Overall Recruitment Status
Completed
Study Start Date
April 2003 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
July 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maastricht University Medical Center
Collaborators
Stryker European Operations BV
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Thr purpose of this study is to compare the clinical and radiological results, as well as the femur bone density measurements of two uncemented total hip prostheses during 5 years of follow up.
Detailed Description
It is of great importance for the function of uncemented total hip arthroplasty that the anchorage of the prosthesis in the bone of the femur is sufficient. This is of great importance in the prevention of stress shielding of the bone and to insure tranfer of forces from the prosthesis to the femur.
The symax hip stem is developed to optimize stress tranfer to bone and insure mechanical stability.
In this study the symax hip stem is compared to the HA_Omnifit hip stem (a frequently used and long term evaluated uncemented hip prosthesis) During the fist two years of follow up DEXA mesurments of bone mineral density are performed. Also patient satisfaction, patient fuction score and radiological evaluation measurements are done during 5 years of follow up.
Our primary objective is: comparison of the short term bone remodelling surrounding the Symax hip stem to the short term remodeling surrounding the Stryker Omnifit HA hip stem measured by bone densitometry, clinical and radiographic evaluation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis
Keywords
uncemented hip, bone remodeling, DEXA, clinical evaluation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
HA-Omnifit
Arm Type
Active Comparator
Arm Description
Patients who receive a HA-Omnifit uncemented hip stem
Arm Title
Symax hip stem
Arm Type
Active Comparator
Arm Description
Patients with the Symax uncemented hip stem
Intervention Type
Procedure
Intervention Name(s)
uncemented total hip arthroplasty
Primary Outcome Measure Information:
Title
short term bone remodeling
Description
Bone remodeling is determined by measuring the Bone mineral density during time
Time Frame
6 times within 2 years
Title
complications and reoperations
Description
Reporting all complications and reoperations of the two different hip prostheses
Time Frame
during 5 years
Secondary Outcome Measure Information:
Title
clinical performance
Description
Comparison of the clinical performance of the two different hip prostheses
Time Frame
9 times within 5 years
Title
Radiological evaluation
Description
Evaluation of Xrays according to the engh classifications
Time Frame
9 times within 5 years
Other Pre-specified Outcome Measures:
Title
patient satisfaction
Description
comparison of patient satisfaction between the two different prostheses
Time Frame
9 times within 5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:Male or non pregnant female patients >18 years
Patient with degenerative or traumatic changes to hip requiring hip replacement
Patient with BMI<35
Patient signed informed consent
Exclusion Criteria:
chronic anti-inflammatory medication use> 3 months
revision surgery to the affected femur
Cancer therapy including immunosuppression, chemotherapy and radiation
Pathological fractures, delayed ossification or non-union is likely to occur
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lodewijk van Rhijn
Organizational Affiliation
azM
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
24378381
Citation
ten Broeke RH, Tarala M, Arts JJ, Janssen DW, Verdonschot N, Geesink RG. Improving peri-prosthetic bone adaptation around cementless hip stems: a clinical and finite element study. Med Eng Phys. 2014 Mar;36(3):345-53. doi: 10.1016/j.medengphy.2013.12.006. Epub 2013 Dec 27.
Results Reference
derived
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RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hip Stem
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