Cemented Versus Uncemented Stems in Total Hip Arthroplasty in Patients With Femoral Neck Fractures
Primary Purpose
Femoral Neck Fractures
Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Total Hip Arthroplasty
Cemented Lubinus SPII stem (control arm)
Uncemented HA Coated Corail stem
Sponsored by
About this trial
This is an interventional treatment trial for Femoral Neck Fractures focused on measuring Femoral neck fractures, Uncemented, Hydroxyapatite, Coated, Femoral, Stems, Hip fractures, THA, THR, Cemented, Fat embolism, Cognition, Inflammatory response, Mobilization
Eligibility Criteria
Inclusion Criteria:
- Patients who are acutely admitted to hospital with dislocated femoral neck fractures, that in clinical praxis are in the need of hip prosthesis surgery, are recruited in the study. The fracture shall not engage the lesser nor the greater trochanters.
- Patients who wants to participate in the study and who can consider participation for at least 1 year.
- Coming from independent dwelling conditions.
- Not dementia.
- Circa 60-85 years of age.
- Circa 50 patients in each arm/group shall be included at Mölndal's Hospital (part of Sahlgrenska University Hospital).
Exclusion Criteria:
- Patients who have difficulties in understanding the intent of the study.
- Rheumatic disorders (RA, Bechterew, SLE).
- Cortison treatment.
- Stroke with remaining weakness or neurological disorders with affection of locomotion.
- Dementia.
- Grave obesity with BMI >=30-35.
- Delay between time of injury and time of surgery exceeding 72 hours.
Sites / Locations
- Mölndals Hospital (part of Sahlgrenska University Hospital)
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Uncemented HA Coated Corail stem
Cemented Lubinus SPII stem (control arm)
Arm Description
Surgery with an inversed hybrid arthroplasty with an uncemented hydroxyapatite coated Corail stem and a cemented Marathon cup (DePuy).
Surgery with a totally cemented option with a Lubinus SPII stem and a IP cup (Link).
Outcomes
Primary Outcome Measures
Time to mobilization.
Time (days) to mobilization defined as independent walking with or without walking aids measured by ward physiotherapist with Traffic Light System and Sahlgrenska University Hospital Hip Score (SUHS).
Secondary Outcome Measures
Cognitive status. Eventual confusion.
Cognitive status measured once daily with Pfeiffer's test (Short Portable Mental Status Questionnaire - SPMSQ).
Eventual confusion is noted once daily.
Oxygen saturation levels peroperatively.
POX-measurements during different phases of surgery along with pulmonary catheter readings.
Bone remodeling around the hip prosthesis.
Measurements with hip DXA.
Biomarkers / inflammatory response.
Blood samples for measurement of the inflammatory response with biochip multi-array technology.
Fixation / migration / loosening of the hip prosthesis components.
Measured by radiostereometric analysis (RSA) in addition to the conventional pelvis and hip X-ray exams. Early radiological loosening of one or both of the prosthesis components is identified at an early stage with RSA.
Reoperation.
In case of for example infection or dislocation.
PROM - Patient Reported Outcome Measurements.
Questionnaires regarding Patient's satisfaction, Quality of life (EQ-5D), Activity level (UCLA), Harris Hip Score.
Full Information
NCT ID
NCT01578408
First Posted
April 11, 2012
Last Updated
September 22, 2020
Sponsor
Sahlgrenska University Hospital, Sweden
Collaborators
DePuy Orthopaedics
1. Study Identification
Unique Protocol Identification Number
NCT01578408
Brief Title
Cemented Versus Uncemented Stems in Total Hip Arthroplasty in Patients With Femoral Neck Fractures
Official Title
Corail-SP Study - A Prospective Randomized Comparison Between Cemented and Uncemented Hydroxyapatite Coated Prosthesis Stems in Total Hip Arthroplasty in Patients With Femoral Neck Fractures
Study Type
Interventional
2. Study Status
Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
May 11, 2010 (Actual)
Primary Completion Date
March 9, 2018 (Actual)
Study Completion Date
February 19, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sahlgrenska University Hospital, Sweden
Collaborators
DePuy Orthopaedics
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this prospective randomized study is to compare the quality of treatment between cemented versus uncemented hydroxyapatite coated femoral stems in Total Hip Arthroplasty (THA) in patients who suffers from dislocated femoral neck fractures.
Our hypothesis is that an uncemented option spares the patient the operative load of the cementing procedure, i e risk of fatty embolism and inflammatory response, which in turn also perhaps reduces the postoperative cognition strain and improves mobilization parameters.
If the uncemented option has the same excellent fixation in poor bone stock, as in the case of these osteopenic fractures, and also has the same good clinical outcome, it would be a viable standard option for the treatment of dislocated femoral neck fractures.
Detailed Description
Corail-SP study. A prospective randomized study to compare the quality of treatment between cemented versus uncemented hydroxyapatite coated femoral stems in Total Hip Arthroplasty (THA) in patients who suffers from dislocated femoral neck fractures.
Femoral neck fractures often occurs among the fragile elderly patients who have a higher degree of co-morbidity. The 3-month mortality is 13%. The incidence of risk of fracture complications when using osteosyntheses are as high as 30-40%, mainly due to non union, which leads to impairments in quality of life, locomotion and pain.
For that reason more patients nowadays are submitted to a cemented hemiarthroplasty or a total hip arthroplasty directly after their injury - at the same time the problem with fatty embolism syndrome has been recognized. When cementing during surgery, the bone marrow is pushed into the blood stream, which can affect the cardiopulmonary function and even the mental functions.
As a measure for reducing those risks an uncemented hip arthroplasty is sometimes used instead.
The pros and cons with uncemented fixation is poorly examined which this study will try to scrutinize.
100 patients with dislocated (Garden classification III-IV) femoral neck fractures who have the clinical indication of undergoing a Total Hip Arthroplasty are asked and included at Mölndals Hospital (part of Sahlgrenska University Hospital).
Randomization to either; an inversed hybrid arthroplasty with an uncemented hydroxyapatite coated Corail stem and a cemented Marathon cup (DePuy), alternatively to, a totally cemented option with a Lubinus SPII stem and a IP cup (Link).
Preoperatively:
Patient questionnaires regarding cognitive and social status, hip function, quality of life (QoL), activity level. Standard hip and pelvis X-ray. Blood sample for biomarkers.
Peroperatively:
Pulmonary artery catheter measurements of pulmonary artery pressure, cardiac output, ejection fraction of the right ventricle. Surgeon's questionnaire regarding prosthesis components, duration of surgery, blood group, bleeding volume, oxygen saturation. Half of the patients are marked with tantalum pellets for radiostereometric analysis (RSA). Biomarkers.
Postoperatively:
Standard X-ray. On the patients marked with tantalum pellets RSA is performed. Bone density scan (DXA). Measurements regarding cognition, ADL, mobilization. Eventual confusion is noted. Biomarkers every second day until discharge from hospital. Eventual wound infections or thromboembolic episodes are noted.
Follow up:
Outpatient return visits to physician 3, 6 months, 1, 2, 5, 7, 10 years postoperatively. Standard X-ray, RSA, DXA, Patient questionnaires regarding patient's satisfaction, QoL, activity level, hip function. Biomarkers.
Eventual gains with an uncemented prosthesis:
Reduced fatty embolism risk, reduced inflammatory response, reduced generalized symptoms/confusion, faster mobilization, shorter surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Femoral Neck Fractures
Keywords
Femoral neck fractures, Uncemented, Hydroxyapatite, Coated, Femoral, Stems, Hip fractures, THA, THR, Cemented, Fat embolism, Cognition, Inflammatory response, Mobilization
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
109 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Uncemented HA Coated Corail stem
Arm Type
Active Comparator
Arm Description
Surgery with an inversed hybrid arthroplasty with an uncemented hydroxyapatite coated Corail stem and a cemented Marathon cup (DePuy).
Arm Title
Cemented Lubinus SPII stem (control arm)
Arm Type
Active Comparator
Arm Description
Surgery with a totally cemented option with a Lubinus SPII stem and a IP cup (Link).
Intervention Type
Procedure
Intervention Name(s)
Total Hip Arthroplasty
Intervention Type
Device
Intervention Name(s)
Cemented Lubinus SPII stem (control arm)
Intervention Description
Cemented Lubinus femoral stem. Cemented IP acetabular cup. (Link).
Intervention Type
Device
Intervention Name(s)
Uncemented HA Coated Corail stem
Intervention Description
Uncemented hydroxyapatite coated Corail femoral stem. Cemented Marathon acetabular cup. (DePuy).
Primary Outcome Measure Information:
Title
Time to mobilization.
Description
Time (days) to mobilization defined as independent walking with or without walking aids measured by ward physiotherapist with Traffic Light System and Sahlgrenska University Hospital Hip Score (SUHS).
Time Frame
During hospital stay, an expected average of 10 days.
Secondary Outcome Measure Information:
Title
Cognitive status. Eventual confusion.
Description
Cognitive status measured once daily with Pfeiffer's test (Short Portable Mental Status Questionnaire - SPMSQ).
Eventual confusion is noted once daily.
Time Frame
During hospital stay, an expected average of 10 days.
Title
Oxygen saturation levels peroperatively.
Description
POX-measurements during different phases of surgery along with pulmonary catheter readings.
Time Frame
Peroperatively (during surgery), an expected average of 2 hours.
Title
Bone remodeling around the hip prosthesis.
Description
Measurements with hip DXA.
Time Frame
Postoperatively in average after 2 days. All follow up visits at 3, 6 months, 1, 2, 5, 7, 10 years.
Title
Biomarkers / inflammatory response.
Description
Blood samples for measurement of the inflammatory response with biochip multi-array technology.
Time Frame
Preoperatively in average 4 hours. Peroperatively at end of wound closure. Postoperatively 1, 3, 5, 7 days. All follow up visits at 3, 6 months, 1, 2, 5, 7, 10 years.
Title
Fixation / migration / loosening of the hip prosthesis components.
Description
Measured by radiostereometric analysis (RSA) in addition to the conventional pelvis and hip X-ray exams. Early radiological loosening of one or both of the prosthesis components is identified at an early stage with RSA.
Time Frame
Postoperatively in average after 2 days. All follow up visits at 3, 6 months, 1, 2, 5, 7, 10 years.
Title
Reoperation.
Description
In case of for example infection or dislocation.
Time Frame
Postoperatively up to 10 years.
Title
PROM - Patient Reported Outcome Measurements.
Description
Questionnaires regarding Patient's satisfaction, Quality of life (EQ-5D), Activity level (UCLA), Harris Hip Score.
Time Frame
Preoperatively in average 4 hours. Postoperatively at discharge from hospital at an expected average of 10 days. All follow up visits at 3, 6 months, 1, 2, 5, 7, 10 years.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients who are acutely admitted to hospital with dislocated femoral neck fractures, that in clinical praxis are in the need of hip prosthesis surgery, are recruited in the study. The fracture shall not engage the lesser nor the greater trochanters.
Patients who wants to participate in the study and who can consider participation for at least 1 year.
Coming from independent dwelling conditions.
Not dementia.
Circa 60-85 years of age.
Circa 50 patients in each arm/group shall be included at Mölndal's Hospital (part of Sahlgrenska University Hospital).
Exclusion Criteria:
Patients who have difficulties in understanding the intent of the study.
Rheumatic disorders (RA, Bechterew, SLE).
Cortison treatment.
Stroke with remaining weakness or neurological disorders with affection of locomotion.
Dementia.
Grave obesity with BMI >=30-35.
Delay between time of injury and time of surgery exceeding 72 hours.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johan Kärrholm, Prof MD PhD
Organizational Affiliation
Orthopaedic Department, Sahlgrenska University Hospital, Gothenburg, SWEDEN
Official's Role
Study Director
Facility Information:
Facility Name
Mölndals Hospital (part of Sahlgrenska University Hospital)
City
Mölndal
ZIP/Postal Code
43180
Country
Sweden
12. IPD Sharing Statement
Learn more about this trial
Cemented Versus Uncemented Stems in Total Hip Arthroplasty in Patients With Femoral Neck Fractures
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