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Metal Ion Levels in Total Hip Arthroplasty (THA) With Modular Dual Mobility Cup Compared to Conventional THA

Primary Purpose

Femur Neck Fracture, Arthroplasty Complications

Status
Active
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Total hip replacement arthroplasty using modular dual mobility cup
Total hip replacement arthroplasty using conventional acetabular cup
Sponsored by
Korea University Guro Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Femur Neck Fracture focused on measuring Total hip arthroplasty, Metal ion, Dual mobility, Total hip replacement

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Over 60 years of age. Femoral neck fracture or hip joint disease. Garden stage III, IV
  2. Comorbidities: American Society of Anesthesiology (ASA) grade III or less, Charlson comorbidity 6 points or less
  3. Daily activity: UCLA score 4 or higher, Koval score 4 or lower
  4. Including patients with neuromuscular disorder and cognitive impairment

Exclusion Criteria:

  1. Revision arthroplasty
  2. In case of factors other than fretting corrosion of the index arthroplasty that can cause an increase in serum metal ion level - In case of undergoing surgery using metal on other joints before this operation, vitamin B user
  3. Patients with abnormal kidney function in which Blood urea nitrogen (BUN) and Cr are out of normal values
  4. Pathologic fracture
  5. If you have metabolic bone disorder, exclude osteoporosis (ex. Paraneoplastic syndrome, renal osteodystrophy, Vit D disorder, hormonal disorder)

Sites / Locations

  • KoreaUGuroH

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Modular dual mobility group

Conventional group

Arm Description

A group of patients who underwent total hip replacement arthroplasty using a modular dual mobility cup

A group of patients who underwent total hip replacement arthroplasty using a conventional acetabular cup

Outcomes

Primary Outcome Measures

Change in Metal ion level
Measurement of metal ion concentration in blood serum

Secondary Outcome Measures

Change in Clinical measurement (Pain-visual analog scale)
Pain-visual analog scale
Change in Clinical measurement (Harris hip score)
Harris hip score
Change in Clinical measurement (Oxford hip score)
Oxford hip score
Change in Clinical measurement (UCLA score)
University of California at Los Angeles (UCLA) activity score
Change in Radiological measurement (Hip x-ray)
Acetabular cup inclination (degree)
Change in Radiological measurement (CT)
Anterior angle (degree, measured by computed tomography)
Change in Radiological measurement (Long leg x-ray)
Leg length difference (mm)
Post operative complication (Dislocation)
Dislocation or not
Post operative complication (Infection)
Infection or not
Post operative complication (Osteolysis)
Osteolysis or not
Post operative complication (Implant dissociation)
Implant dissociation or not
Revision surgery
Revision surgery or not

Full Information

First Posted
December 3, 2021
Last Updated
December 20, 2021
Sponsor
Korea University Guro Hospital
Collaborators
Stryker Korea Co., Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT05181566
Brief Title
Metal Ion Levels in Total Hip Arthroplasty (THA) With Modular Dual Mobility Cup Compared to Conventional THA
Official Title
Metal Ion Levels in Total Hip Arthroplasty (THA) With Modular Dual Mobility (MDM) Cup Compared to Conventional Total Hip Arthroplasty (THA) - A Multicenter Prospective Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 5, 2019 (Actual)
Primary Completion Date
August 3, 2021 (Actual)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Korea University Guro Hospital
Collaborators
Stryker Korea Co., Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
After total hip arthroplasty using an 'Modular Dual Mobility' acetabular cup, which is effective in reducing the risk of dislocation, one of the serious complications occurring after total hip arthroplasty, the blood metal ion concentration was compared with that of conventional total hip arthroplasty patients. This is a multicenter prospective randomized comparative study.
Detailed Description
Dislocation after total hip arthroplasty is a very serious complication not only for the patient but also for the operator, and is the second most common complication after joint dissociation. The incidence of dislocation after conventional total hip arthroplasty has been reported to be about 0.2 to 7%, and the frequency is higher in elderly patients with hip fractures and has been reported up to about 9%. In patients at high risk of dislocation, total hip arthroplasty using a dual mobility acetabular cup has the effect of reducing the risk of dislocation, and its use has been increasing in recent years. The dual mobility acetabular cup used in this study was developed in a form that can be screwed through the acetabular cup to compensate for the shortcomings of the dual mobility acetabular cup used in the past. The modular dual mobility acetabular cup, which can be fixed with screws, has a metal liner inserted therein, so there is a possibility that the concentration of metal ions in the blood may rise. Until now, studies on the concentration of metal ions in the blood after total hip arthroplasty using an modular dual mobility acetabular cup have been reported very rarely, and the results are also reported differently [4-7]. In addition, no prospective comparative study on blood metal ion concentrations after total hip arthroplasty using an modular dual mobility acetabular cup in elderly patients with femoral neck fractures has been reported. The release of metal ions due to metal corrosion or metal friction in the artificial joint is a rare phenomenon, but it can cause serious complications in the body. It has been suggested through case reports that it can cause abnormalities in the nervous system and cardiovascular system by increasing the concentration of metal ions in the body as well as bone complications such as osteolytic artificial joint relaxation pseudotumor around the artificial joint [5-7] , and a comparative analysis of the modular dual mobility acetabular cup with the conventional acetabular cup to see if there is any problem of metal ion rise in the body due to the release of metal ion concentration is a very important and meaningful study for both doctors and patients performing hip arthroplasty. In addition, it is expected that the medical and social contribution of this research will not be small, considering that the artificial prosthesis used as a material for metal-to-metal surface replacement surgery in the hip joint arthroplasty field was recalled a few years ago and caused a big wave around the world. Matsen et al. defined significant elevation when Cobalt ≥ 1.6 mcg/L, based on previous literature that required revision for adverse local tissue reaction (ALTR). A guideline for follow-up of a metal artificial joint is attached as an appendix. Nam et al. (J Arthroplasty, 2016) reported that the frequency of patients with cobalt ion levels deviating from the normal reference values at 1 year after surgery was 4/26 (15.3%), MDM THA vs. 1/17 (5.9%) reported that it was Conventional THA. Matsen et al. did not specify the timing of the initial measurement of the ion concentration, but said that if abnormal values were observed, they were followed continuously every 6 months. Based on the previous literature that required revision for adverse local tissue reaction (ALTR), Cobalt ≥ 1.6 mcg/L was defined as significant elevation. As a result of following 100 patients, it was confirmed that the cobalt concentration was outside the normal range in 21 patients (21%), and a significant increase in the cobalt ion concentration of 1.6 mcg/L or more was reported in 9 patients (9%). And two of them had ALTR on MRI. Metal ions can be released and the concentration of metal ions in the body can be increased in not only artificial joint replacement surgery using the assembled double movable acetabular cup but also in the solid acetabular cup. The acetabular cup and the femoral stem may be worn during joint movement due to the collision phenomenon, and if the acetabular cup screw is loosened or incorrectly inserted and corroded and worn, metal ions may be released along with the surrounding osteolysis. The reason for performing randomization in this study is first, to ensure that the subject's characteristics do not affect the group to be assigned, so that the probability that each subject will receive surgery with which of the two substitutes is equally applied. , Second, in order to maximize the internal validity of the research results, to make the characteristics of the subjects to which the substitutes to be compared belong to be as similar as possible except for the substitutes assigned to them. Third, since statistical analysis was developed based on the theory of probability, The reason for randomizing the assignment of study subjects to the substitutions used is because it satisfies the prerequisites for applying statistical techniques to the analysis of research data. Comparing and analyzing the difference in the concentration of metal ions in the blood through randomization is an important study that can confirm whether the difference in metal ion release can be caused by the difference in the binding mechanism between the two acetabular cups. It is an important complication after joint arthroplasty that can cause side effects and can cause harm to internal organs or revision surgery. Therefore, analyzing it is very important and meaningful research. The purpose of this study was to compare the blood metal ion concentration in elderly patients after total hip arthroplasty using an modular dual mobility acetabular cup with the results of the conventional total hip arthroplasty patient group in a multicenter prospective study. In addition, we intend to compare clinical and radiological factors that are commonly evaluated during outpatient follow-up after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Femur Neck Fracture, Arthroplasty Complications
Keywords
Total hip arthroplasty, Metal ion, Dual mobility, Total hip replacement

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Modular dual mobility group
Arm Type
Experimental
Arm Description
A group of patients who underwent total hip replacement arthroplasty using a modular dual mobility cup
Arm Title
Conventional group
Arm Type
Active Comparator
Arm Description
A group of patients who underwent total hip replacement arthroplasty using a conventional acetabular cup
Intervention Type
Procedure
Intervention Name(s)
Total hip replacement arthroplasty using modular dual mobility cup
Intervention Description
In a total hip replacement (also called total hip arthroplasty), the damaged bone and cartilage is removed and replaced with prosthetic components
Intervention Type
Procedure
Intervention Name(s)
Total hip replacement arthroplasty using conventional acetabular cup
Intervention Description
In a total hip replacement (also called total hip arthroplasty), the damaged bone and cartilage is removed and replaced with prosthetic components
Primary Outcome Measure Information:
Title
Change in Metal ion level
Description
Measurement of metal ion concentration in blood serum
Time Frame
Baseline (pre op.), post op. 12 months
Secondary Outcome Measure Information:
Title
Change in Clinical measurement (Pain-visual analog scale)
Description
Pain-visual analog scale
Time Frame
Post op. 6 months, post op. 12 months, post op. 24 months
Title
Change in Clinical measurement (Harris hip score)
Description
Harris hip score
Time Frame
Post op. 6 months, post op. 12 months, post op. 24 months
Title
Change in Clinical measurement (Oxford hip score)
Description
Oxford hip score
Time Frame
Post op. 6 months, post op. 12 months, post op. 24 months
Title
Change in Clinical measurement (UCLA score)
Description
University of California at Los Angeles (UCLA) activity score
Time Frame
Post op. 6 months, post op. 12 months, post op. 24 months
Title
Change in Radiological measurement (Hip x-ray)
Description
Acetabular cup inclination (degree)
Time Frame
Baseline (immediate post op.), post op. 6 months, post op. 12 months, post op. 24 months
Title
Change in Radiological measurement (CT)
Description
Anterior angle (degree, measured by computed tomography)
Time Frame
Baseline (immediate post op.), post op. 6 months, post op. 12 months, post op. 24 months
Title
Change in Radiological measurement (Long leg x-ray)
Description
Leg length difference (mm)
Time Frame
Baseline (immediate post op.), post op. 6 months, post op. 12 months, post op. 24 months
Title
Post operative complication (Dislocation)
Description
Dislocation or not
Time Frame
Baseline (immediate post op.), post op. 6 months, post op. 12 months, post op. 24 months
Title
Post operative complication (Infection)
Description
Infection or not
Time Frame
Baseline (immediate post op.), post op. 6 months, post op. 12 months, post op. 24 months
Title
Post operative complication (Osteolysis)
Description
Osteolysis or not
Time Frame
Baseline (immediate post op.), post op. 6 months, post op. 12 months, post op. 24 months
Title
Post operative complication (Implant dissociation)
Description
Implant dissociation or not
Time Frame
Baseline (immediate post op.), post op. 6 months, post op. 12 months, post op. 24 months
Title
Revision surgery
Description
Revision surgery or not
Time Frame
Baseline (immediate post op.), post op. 6 months, post op. 12 months, post op. 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Over 60 years of age. Femoral neck fracture or hip joint disease. Garden stage III, IV Comorbidities: American Society of Anesthesiology (ASA) grade III or less, Charlson comorbidity 6 points or less Daily activity: UCLA score 4 or higher, Koval score 4 or lower Including patients with neuromuscular disorder and cognitive impairment Exclusion Criteria: Revision arthroplasty In case of factors other than fretting corrosion of the index arthroplasty that can cause an increase in serum metal ion level - In case of undergoing surgery using metal on other joints before this operation, vitamin B user Patients with abnormal kidney function in which Blood urea nitrogen (BUN) and Cr are out of normal values Pathologic fracture If you have metabolic bone disorder, exclude osteoporosis (ex. Paraneoplastic syndrome, renal osteodystrophy, Vit D disorder, hormonal disorder)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sangmin Kim, Ph.D
Organizational Affiliation
Korea University Guro Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
KoreaUGuroH
City
Seoul
ZIP/Postal Code
08308
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
No

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Metal Ion Levels in Total Hip Arthroplasty (THA) With Modular Dual Mobility Cup Compared to Conventional THA

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