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Hip Fractures Treated With Uncemented Arthroplasties

Cemented Versus Uncemented Arthroplasty in Elderly Patients With Displaced Femoral Neck Fractures: a Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01798472
Acronym
HUA
Enrollment
140
Registered
2013-02-25
Start date
2009-11-30
Completion date
2018-11-30
Last updated
2015-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Femoral Neck Fractures

Keywords

displaced femoral neck fractures, treatment, uncemented arthroplasty, cemented arthroplasty

Brief summary

The aim of this study is to compare the functional and radiological outcome after displaced, femoral neck fractures treated with either cemented or uncemented arthroplasties. The primary hypothesis is that the uncemented arthroplasty shows the same functional outcome at 12 month as the cemented arthroplasty.

Detailed description

Femoral neck fracture is a common cause of suffering and premature mortality among the elderly. Riskfactors for femoral neck fractures are age, gender, osteoporosis and cognitive dysfunction. Mortality and morbidity varies between undisplaced and displaced femoral neck fractures. Different treatment options are available: reduction and internal fixation vs joint replacement (arthroplasty). The treatment of undisplaced femoral neck fractures is uncontroversial and consists of internal fixation with screws. The treatment of displaced, femoral neck fractures with internal fixation shows unacceptable results with complications rates leading to reoperation between 40-60%. Treatment of these fractures with arthroplasties has therefore become the standard treatment in industrial countries. Fixation of the femoral component with bone-cement is standard procedure in Europe today. To avoid negative cardio-pulmonary events in patients with serious comorbidities and in very old and frail patients uncemented femoral components or internal fixation are used. These uncemented stems are mostly older design with poor track records. The use of modern, well-documented stems used in an osteoarthritis population for fracture patients has still to be tested.

Interventions

Patients aged 80 years and older operated with an cemented hemiarthroplasty. Fixation of the wedge-shaped, polished ChromCobalt steel femoral stem to host bone by use of PolyMetylMetAcrylat bone cement. The acetabulum is not replaced. The prosthesis articulates with the patients acetabulum with an unipolar, femoral head made of ChromCobalt steel.

PROCEDUREreverse hybrid total hip arthroplasty

Patients aged 65 to 79 years operated with an uncemented femoral component combined with cemented acetabular cup. The femoral stem is fixed to the host bone by press-fit technique. We use a tapered, proximally hydroxyapatite coated, titanium stem. The acetabular cup is fixed to the host bone with bone cement. We use an all-polyethylene design. Bone cement consists of PolyMetylMetAcrylat.

Patients aged 65 to 79 years operated with a cemented femoral stem combined with a cemented acetabular cup. Femoral and acetabular component are fixed to the host bone by use of bone cement. The femoral stem is a polished, wedge-shaped design made of ChromCobalt steel. The acetabular cup is fixed to the host bone with bone cement.The acetabular cup an all-polyethylene design. Bone cement consists of PolyMetAcrylat.

PROCEDUREuncemented hemiarthroplasty

Patients aged 80 years and older are randomized to uncemented hemiarthroplasty. Fixation of the tapered, proximally hydroxyapatite coated, titanium stem to the host bone by press-fit-technique. The acetabulum is not replaced. The prosthesis articulates with the patients acetabulum with an unipolar, femoral head made of ChromCobalt steel.

Sponsors

Karolinska Institutet
CollaboratorOTHER
Stockholm South General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* displaced fracture of the femoral neck * independent living * independent ambulation (with or without walking aids)

Exclusion criteria

* pathological fracture * severe dementia (defined as ≤3 in short portable mental questionnaire) preoperatively * preexisting ipsilateral hip disease * neurological disease (e.g. M. Parkinson) * psychiatric disease which makes understanding or following instructions impossible * history of drug and alcohol abuse

Design outcomes

Primary

MeasureTime frameDescription
Harris Hip Score12 monthOur primary outcome variable is the Harris Hip Score at 12 month follow up. Harris Hip Score is an investigator reported tool evaluating hip function in four dimensions: Pain, function, absence of deformity and range of motion

Secondary

MeasureTime frameDescription
Health related quality of life12 monthWe use the patient reported instrument EQ-5D. A questionnaire consisting of 5 questions to evaluate health related quality of life.
Radiological follow up12 monthEvaluation of radiological outcome on standard hip radiographies with focus on bony ingrowth, signs of loosening and subsidence

Other

MeasureTime frameDescription
General and surgical complicationsfrom operation until 12 month postoperativelygeneral complications such as cardio-pulmonary events, pressure ulcer, pneumonia, deep vein thrombosis (DVT). surgical complications such as infections, reoperations due to all causes, dislocations

Countries

Sweden

Contacts

Primary ContactChristian Inngul, MD
christian.inngul@sodersjukhuset.se0046708355969

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026