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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
Maastricht University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    September 25, 2012
    Last Updated
    September 25, 2012
    Sponsor
    Maastricht University Medical Center
    Collaborators
    Stryker European Operations BV
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    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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