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The Hip Fracture Surgical Approach Trial

The Hip Fracture Surgical Approach Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06146205
Acronym
HIFSAT
Enrollment
476
Registered
2023-11-24
Start date
2024-04-30
Completion date
2028-03-30
Last updated
2026-03-30

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

Conditions

Hip Fracture, Femoral Neck Fracture

Keywords

Fragility fracture, Surgical approach, Hemiarthroplasty, SPAIRE, Direct Lateral Approach, Hip Surgery

Brief summary

The HIFSAT study will compare the standard direct lateral approach to hemiarthroplasty to a new muscle sparing approach (SPAIRE) in femoral neck fracture patients.

Detailed description

Femoral neck fractures are mostly treated with a hemiarthroplasty, where the fractured femoral head is replaced with a metal implant. The most common surgical approach to hemiarthroplasty has been the lateral approach, in which the gluteus medius tendon is partially released from the greater trochanter. Hip pain and limping is not uncommon after this approach has been used. A new surgical approach (SPAIRE) has been developed to alleviate this problem, and in this method the surgeon approaches the injured hip joint from posterior, preserving most of the muscles and tendons around the hip. This trial is designed to assess if this new SPAIRE approach leads to better results than the lateral approach in patients with femoral neck fractures.

Interventions

The hip joint is approached from laterally, and parts of the gluteus medius tendon is released from the greater trochanter before the hip joint is entered from the anterior side.

PROCEDURESPAIRE

The hip joint is entered from posterior, and the approach preserves the external rotators of the hip joint.

Sponsors

Diakonhjemmet Hospital
Lead SponsorOTHER
Oslo University Hospital
CollaboratorOTHER
University Hospital, Akershus
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Femoral neck fracture * Clinical indication for hemiarthroplasty * Age over 50 years

Exclusion criteria

* Previous hip implants in the same hip * Patients assessed to be in a terminal state with an expected survival of less than 1 week * Other factors that makes follow-up impossible

Design outcomes

Primary

MeasureTime frameDescription
Harris Hip Score ( HHS)4 monthsHarris Hip Score (HHS) is an outcome measure for hip-related symptoms. The score is based on both patient-reported information and clinical examination, and is administered by a qualified health care professional. It covers four domains: Pain, function, absence of deformity and range of motion. The score ranges from 0 (worst) to 100 (best).

Secondary

MeasureTime frameDescription
Harris Hip Score (HHS)12 and 24 monthsHarris Hip Score (HHS) is an outcome measure for hip-related symptoms. The score is based on both patient-reported information and clinical examination, and is administered by a qualified health care professional. It covers four domains: Pain, function, presence of deformity and range of motion. The score ranges from 0 (worst) to 100 (best).
Oxford Hip score4,12 and 24 monthsOxford Hip Score(OHS) is a patient reported outcome measure( PROM), OHS is designed to assess outcome after total hip replacement. It has 6 questions on pain and 6 questions on mobility. 5 categories of answer from worst to best. The range is 0-48.
EuroQol-5d-5l4,12 and 24 monthsEuroQol-5d-5l is a descriptive system comprises 5 dimensions: Mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the 5 dimensions can be combined into a 5-digit number that describes the patient's health state, and these digits can be converted into a single numerical value reflecting how the health state is according to the preferences of the general population of a country/region.
Trendelenburg test4,12 and 24 monthsThis is a test to identify weakness in gluteal muscles, that can be seen in patients after hip surgery. Unilateral weakness in the gluteal muscles can for instance because nerve damage, trauma to the muscle or rupture of the tendon. The test will be performed as described by Hardcastle and Wade. The patient will be asked to raise their foot from the ground with 30º of hip flexion. The patient will be instructed to raise the non-stance side of the pelvis as high as possible with the examiner supporting the patient by holding their hands if needed. If the patient is not able to maintain this position for 30 seconds, or not being able to raise the hip of the non-stance side to above the level of the stance-side, the Trendelenburg test is considered positive.
New Mobility Score (NMS)4,12 and 24 monthsNMS consists of 3 questions about ambulation indoor, outdoor and the ability to go shopping. Each question has 4 alternative answers yielding 0-3 points, and the maximum score is 9.
Short Physical Performance Battery (SPPB)4, 12, an 24 monthsThe Short Physical Performance Battery is an assessment tool made specific for screening of physical function among older adults. SPPB has 3 different tests: Balance, walking speed and rising from a chair. Scorings range from 0-12, best possible is 12.
Numerical Pain Rate Scale( NPRS)4, 12 and 24 monthsUnidimensional measure of pain intensity in adults, describing pain extreme from 0 no pain at all to 10 the worst pain imaginable.
Duration of surgery1.st day after surgeryDuration of the operation in minutes
Preferred Walking Speed4,12 and 24 monthsA four-meter distance is marked on the floor, and the patients are instructed to walk this distance in their normal speed, as if they were walking down a street. The distance is walked twice, and the fastest speed is recorded. The subject can use any walking aids, and this is recorded.
Repeated Chair Stand Test4,12 and 24 monthsIn the repeated chair stand test the participants are asked to fold their arms across their chest (the armrests shall not be not used) and stand up from the chair 5 times. This is timed by the examiner, and points are given from 0 to 4
Cumulated Ambulation Score1-5 days after surgeryThis will be recorded at day 1-3 for all patients. This score assesses the patients' early mobility by evaluating their ability to rise from bed, rise from a chair and walk indoor (walking aids permitted).
Timed up and go test4,12 and 24 monthsThis test measures the time that the person uses to rise from a chair, walk three meters, turn around and walk back to the chair, and sit down again, turning 180 degrees. The person can use any mobility aids that he/she would normally use. The TUG test is being scored by the total time measured
Use of analgesia during admission1. day after surgeryAnalgesia during the first calendar day after surgery will be recorded as morphine equivalents according to a calculation table published by the Norwegian Directorate of Health.
Adverse events0-24 monthsAny adverse events will be recorded during the whole study period
Days Alive At Home (DAH)4,12 and 24 monthsDays alive and at home will be measured at 4,12 and 24 months. Patients wish to stay most of their lives at home, this measurement will tell us how long they could stay home and if they came home after their hip fracture.

Countries

Norway

Contacts

STUDY_CHAIRSiri Lillegraven, PhD

Diakonhjemmet Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026