Osteoarthritis, Hip Clinical Trial
Official title:
Evaluation of a Short Femoral Stem in Total Hip Arthroplasty. A Comparative Study on Stability, Bone Remodelling and Patient Outcome.
NCT number | NCT02743208 |
Other study ID # | 2015/846 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | September 2019 |
Est. completion date | September 2021 |
Verified date | December 2019 |
Source | St. Olavs Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In recent years, short femoral stems have been introduced. Short stems are designed based on
traditional stems with good clinical results. The assumed benefit of short stems is that they
are easier to use in mini-invasive surgery, and that preservation of proximal periprosthetic
bone stock is better. Preservation of periprosthetic bone in the proximal femur is thought to
secure long time anchoring of the implant, and reduce the risk of loosening. In addition, a
good proximal bone stock makes later revision surgery less technically demanding. However,
the short stem design could compromise the stability of the prosthesis, and there has been
reported diverging results regarding correct positioning of short stems. This may be due to
the lack of inherent aiming provided by the tip of the traditional long stems. We want to
clinically evaluate the stability and bone remodelling pattern of a new short femoral stem
based on a standard stem with excellent long time results. In addition we will compare the
two different stems regarding positioning, when using a newly developed guiding broach for
the short stem, and the standard broach for the long stem. Finally, patient reported clinical
outcome scores will be evaluated with respect to implant and biomechanical reconstruction.
The aim of this study is to evaluate whether this specific short femoral stem is stable, safe
to use, and if it provides the expected beneficial effects on bone remodelling.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | September 2021 |
Est. primary completion date | September 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years to 70 Years |
Eligibility |
Inclusion Criteria: - receiving primary total hip arthroplasty due to osteoarthritis, posttraumatic arthritis, avascular necrosis, or developmental hip dysplasia (Crowe grade 1) Exclusion Criteria: - osteoporosis - pregnancy - musculoskeletal problems compromising rehabilitation - corticosteroid treatment - dementia - developmental dysplasia (Crowe grade II-IV) - osteosynthesis in place - revision surgery - joint infection - malignancy of the femur/pelvis |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
St. Olavs Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in periprosthetic bone mineral density (BMD) | Postoperative change in BMD following bone remodelling measured by dual-energy x-ray absorptiometry (DXA) | 2 years | |
Secondary | Migration of femoral stem | Migration of femoral stem measured by radiostereometric analysis (RSA) | 2 years | |
Secondary | Biomechanical reconstruction of hip anatomy | Biomechanical key measures in hip anatomy after reconstruction of the hip joint, compared to native anatomy in contralateral hip is analysed on a metric scale to compare the following positions: Horizontal centre of rotation. Vertical centre of rotation. Horizontal femoral offset. Vertical femoral offset. Abductor lever arm. Limb length. Stem-shaft angle, or valgus/varus. | 2 years | |
Secondary | Hip disability osteoarthritis outcome score (HOOS) | 2 years | ||
Secondary | Harris hip score | 2 years | ||
Secondary | Health-related quality of life (EQ-5D). | 2 years |
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