Surgical Approach of Hemiarthroplasty After Femoral Neck Fracture: Posterolateral or Direct Lateral (APOLLO)
Primary Purpose
Hip Fractures, Surgical Approach, Hemiarthroplasty
Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Surgical approach
Sponsored by
About this trial
This is an interventional treatment trial for Hip Fractures
Eligibility Criteria
Inclusion Criteria:
- ≥ 18 years at time of trauma
- Acute hip fracture
- Hemiarthroplasty as recommended treatment according the national guidelines
- Dutch or English fluency and literacy
- Informed consent or by proxy in patients with mental impairment
Exclusion Criteria:
- Multi-trauma-patient (ISS > 15)
- Secondary surgery after failed internal fixation
- Patients with a known metastatic disease and a confirmed pathological fracture of the hip
- Fracture > 7 days at time of surgery
- High risk of non-compliance/adherence to study procedures (e.g. no Dutch residency during follow-up period, or other factors that impair follow-up data collection)
Sites / Locations
- Onze Lieve Vrouwe Gasthuis
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Posterolateral
Direct lateral
Arm Description
Patients treated with a hemiarthroplasty using the posterolateral approach
Patients treated with a hemiarthroplasty using the direct lateral approach
Outcomes
Primary Outcome Measures
EQ-5D-5L
The EQ-5D-5L descriptive system assesses health in five dimensions (MOBILITY, SELF-CARE, USUAL ACTIVITIES, PAIN / DISCOMFORT, ANXIETY / DEPRESSION), each of which has five levels of response (no problems, slight problems, moderate problems, severe problems, extreme problems/unable to). This part of the EQ-5D questionnaire provides a descriptive profile that can be used to generate a health state profile. Health state index scores generally range from less than 0 (where 0 is the value of a health state equivalent to dead; negative values representing values as worse than dead) to 1 (the value of full health), with higher scores indicating higher health utility. The second part of the questionnaire consists of a visual analogue scale (VAS) on which the patient rates his/her perceived health from 0 (the worst imaginable health) to 100 (the best imaginable health).
Secondary Outcome Measures
Re-interventions
Number of patients which are undergoing a re-intervention in the first 6 months after surgery
SPPB
Balance test (SPPB)
FES-I
The Falls Efficacy Scale-International (FES-I) is a short, easy to administer tool that measures the level of concern about fallingduring 16 social and physical activities inside and outside the home whether or not the person actually does the activity. The minimum score is 16 (no concern about falling) to the maximum score of 64 (severe concern about falling).
NRS
Numeric Rating Scale (NRS) is a numeric scale to assess pain. The minimum score is 0 (no pain) and the maximum score is 10 (the worst imaginable pain)
KATZ
Katz Index of Independence in Activities of Daily Living (ADL) is an instrument to assess functional status as a measurement of the client's ability to perform activities of daily living independently. The Index ranks adequacy of performance in the six functions of bathing, dressing, toileting, transferring, continence, and feeding. Clients are scored yes/no for independence in each of the six functions. A score of 6 indicates full function, 4 indicates moderate impairment, and 2 or less indicates severe functional impairment.
Mobility
Mobility according to the mobility score. We'll assess the mobility according to the following options: no walking aids, 1 walking stick, walker or two crutches, in-house mobility but outside no mobility without aids, no functional mobility
Complications
The number of post-operative complications
Discharge destination
Discharge destination: We'll ask where the patient is going to live after discharge, which we compare with the place where the patient was living before the trauma. The options are: independently at home, at home with care, nursing home, rehabilitation center.
Cost-effectiveness
An economic evaluation will be performed for physical functioning and Quality Adjusted Life Years (QALYs). For estimating QALYs, the patients' EQ-5D-5L health states will be converted into utility scores using the Dutch tariff. QALYs will subsequently be calculated using linear interpolation between measurement points.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04438226
Brief Title
Surgical Approach of Hemiarthroplasty After Femoral Neck Fracture: Posterolateral or Direct Lateral
Acronym
APOLLO
Official Title
Surgical Approach of Hemiarthroplasty After Femoral Neck Fracture: Posterolateral or Direct Lateral
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
December 1, 2017 (Actual)
Primary Completion Date
January 7, 2022 (Actual)
Study Completion Date
July 7, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
JointResearch
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Rationale: In the Netherlands the two main surgical approaches for hemiarthroplasty are the posterolateral and the direct lateral approach. Currently there is no conclusive evidence which of these two approaches results in better patient outcomes.
Objective: Assessing the patient outcome comparing the posterolateral with the direct lateral approach in patients being treated with cemented hemiarthroplasty after femoral neck fractures.
Study design: A randomised controlled multi-center superiority trial and natural experiment with an economic evaluation alongside.
Study population: All patients older than 18 years with a femoral neck fracture whereby treatment with cemented hemiarthroplasty is recommended according the national guidelines.
Intervention: Treatment with cemented hemiarthroplasty using the posterolateral approach.
Standard intervention to be compared to: Treatment with cemented hemiarthroplasty using the direct lateral approach.
Main study parameters/endpoints: The primary outcome is the patient-rated quality of life (EQ-5D-5L) at 6 months after surgery.
Secondary outcomes are: ADL functionality (KATZ), Balance test (SPPB), Tendency to Fall (FES-I), Pain (NRS), Re-interventions, Mobility, Discharge destination, Complications, and cost-effectiveness.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The different approaches in the two treatment arms of the randomised controlled trial are widely used techniques in the Netherlands and many of the outcome measures are part of the standard clinical follow-up after hip fracture. Therefore, there is no extra risk or burden for participating patients, except for the time to complete some additional follow-up measurements. The primary outcome measurement and secondary outcomes, will be assessed through questionnaires online, by hardcopy or by phone at baseline, 4 weeks, 3 and 6 months postoperatively. The assessment of the Short Physical Performance Battery (SPPB) balance test, will be performed by one of the study researchers or nurse practitioner to protect continuity and feasibility.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hip Fractures, Surgical Approach, Hemiarthroplasty, Posterolateral, Direct Lateral
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
555 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Posterolateral
Arm Type
Experimental
Arm Description
Patients treated with a hemiarthroplasty using the posterolateral approach
Arm Title
Direct lateral
Arm Type
Experimental
Arm Description
Patients treated with a hemiarthroplasty using the direct lateral approach
Intervention Type
Procedure
Intervention Name(s)
Surgical approach
Intervention Description
The surgical approach of hemiarthroplasty after femoral neck fracture
Primary Outcome Measure Information:
Title
EQ-5D-5L
Description
The EQ-5D-5L descriptive system assesses health in five dimensions (MOBILITY, SELF-CARE, USUAL ACTIVITIES, PAIN / DISCOMFORT, ANXIETY / DEPRESSION), each of which has five levels of response (no problems, slight problems, moderate problems, severe problems, extreme problems/unable to). This part of the EQ-5D questionnaire provides a descriptive profile that can be used to generate a health state profile. Health state index scores generally range from less than 0 (where 0 is the value of a health state equivalent to dead; negative values representing values as worse than dead) to 1 (the value of full health), with higher scores indicating higher health utility. The second part of the questionnaire consists of a visual analogue scale (VAS) on which the patient rates his/her perceived health from 0 (the worst imaginable health) to 100 (the best imaginable health).
Time Frame
at 6 months after surgery
Secondary Outcome Measure Information:
Title
Re-interventions
Description
Number of patients which are undergoing a re-intervention in the first 6 months after surgery
Time Frame
at 6 months after surgery
Title
SPPB
Description
Balance test (SPPB)
Time Frame
at 4 months after surgery
Title
FES-I
Description
The Falls Efficacy Scale-International (FES-I) is a short, easy to administer tool that measures the level of concern about fallingduring 16 social and physical activities inside and outside the home whether or not the person actually does the activity. The minimum score is 16 (no concern about falling) to the maximum score of 64 (severe concern about falling).
Time Frame
at 6 months after surgery
Title
NRS
Description
Numeric Rating Scale (NRS) is a numeric scale to assess pain. The minimum score is 0 (no pain) and the maximum score is 10 (the worst imaginable pain)
Time Frame
at 6 months after surgery
Title
KATZ
Description
Katz Index of Independence in Activities of Daily Living (ADL) is an instrument to assess functional status as a measurement of the client's ability to perform activities of daily living independently. The Index ranks adequacy of performance in the six functions of bathing, dressing, toileting, transferring, continence, and feeding. Clients are scored yes/no for independence in each of the six functions. A score of 6 indicates full function, 4 indicates moderate impairment, and 2 or less indicates severe functional impairment.
Time Frame
at 6 months after surgery
Title
Mobility
Description
Mobility according to the mobility score. We'll assess the mobility according to the following options: no walking aids, 1 walking stick, walker or two crutches, in-house mobility but outside no mobility without aids, no functional mobility
Time Frame
at 6 months after surgery
Title
Complications
Description
The number of post-operative complications
Time Frame
During admission, 3 and 6 months post-operative
Title
Discharge destination
Description
Discharge destination: We'll ask where the patient is going to live after discharge, which we compare with the place where the patient was living before the trauma. The options are: independently at home, at home with care, nursing home, rehabilitation center.
Time Frame
After admission, at 3 and 6 months post-operative
Title
Cost-effectiveness
Description
An economic evaluation will be performed for physical functioning and Quality Adjusted Life Years (QALYs). For estimating QALYs, the patients' EQ-5D-5L health states will be converted into utility scores using the Dutch tariff. QALYs will subsequently be calculated using linear interpolation between measurement points.
Time Frame
at 4 weeks, 3 and 6 months post-operative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
≥ 18 years at time of trauma
Acute hip fracture
Hemiarthroplasty as recommended treatment according the national guidelines
Dutch or English fluency and literacy
Informed consent or by proxy in patients with mental impairment
Exclusion Criteria:
Multi-trauma-patient (ISS > 15)
Secondary surgery after failed internal fixation
Patients with a known metastatic disease and a confirmed pathological fracture of the hip
Fracture > 7 days at time of surgery
High risk of non-compliance/adherence to study procedures (e.g. no Dutch residency during follow-up period, or other factors that impair follow-up data collection)
Facility Information:
Facility Name
Onze Lieve Vrouwe Gasthuis
City
Amsterdam
State/Province
Noord Holland
ZIP/Postal Code
1090 HM
Country
Netherlands
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Surgical Approach of Hemiarthroplasty After Femoral Neck Fracture: Posterolateral or Direct Lateral
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