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Hemiarthroplasty or Internal Fixation for Displaced Femoral Neck Fractures - 5 Years Follow up

Hemiarthroplasty or Internal Fixation for Displaced Femoral Neck Fractures - 5 Years Follow up

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00764153
Enrollment
222
Registered
2008-10-01
Start date
2002-10-31
Completion date
2011-12-31
Last updated
2014-10-23

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, Function, Pain, Quality of life, Complications, Reoperations, Internal Fixation, Hemiarthroplasty, Activities of Daily Living

Brief summary

An estimated 1.6 million patients sustain a hip fracture every year, about half of these are intracapsular femoral neck fractures. A femoral neck fracture is a life changing event for any patient, and the risk of disability, increased dependence and death is substantial. The main treatment options for displaced femoral neck fractures are internal fixation and arthroplasty. It is established that there are more complications and reoperations after internal fixation, and better short term clinical results with arthroplasty, but knowledge about long term results is lacking.

Detailed description

Patients were included from 2002-2004. Two years follow up was finished by 2006. Patients with displaced intracapsular femoral neck fractures were included and randomized by means of closed numbered envelopes to operation groups: 1. Two parallel screws (Olmed). 2. Hemiarthroplasty with Charnley/ Hastings prosthesis. A priori one would expect that there would be less morbidity and mortality with the less extensive and quicker operation with parallel screw and that a faster and better rehabilitation would be achieved with hemiarthroplasty.

Interventions

Lateral approach. FWB.

Fluoroscopic Control. Percutaneous. FWB. Two parallel screws (Olmed)

Sponsors

Norwegian Foundation for Health and Rehabilitation
CollaboratorOTHER
The Research Council of Norway
CollaboratorOTHER
Ullevaal University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Displaced femoral neck fracture * Age 60 or above * Able to walk (any aids allowed)

Exclusion criteria

* Anesthesiologically unfit for arthroplasty surgery * Previous symptomatic hip pathology (i.e. arthritis) * Pathological fracture * Delay of more than 96 hours from injury to treatment * Not living in hospital area

Design outcomes

Primary

MeasureTime frame
Harris Hip Score5-6 years

Secondary

MeasureTime frame
Eq-5d5-6 years
Barthel Index5-6 years
Reoperations and complications5-6 years

Outcome results

None listed

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