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Clinical Investigation Comparing Two Different Ultra-porous Coated Surfaces of Uncemented Cups

Primary Purpose

Osteoarthritis, Hip

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
MobilLINK TrabecuLINK cup
Pinnacle Gription cup
Sponsored by
Umeå University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Hip focused on measuring Osteoarthritis, Total hip arthroplasty, Uncemented total hip arthroplasty

Eligibility Criteria

30 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients are foreseen for implantation of an uncemented acetabular press-fit cup and an uncemented stem Age 30-70 years Primary osteoarthritis of the hip Body Mass Index between 18 and 35 kg/m2 Willingness and ability to follow clinical investigation protocol Exclusion Criteria: Grossly abnormal hip anatomy (hip dysplasia, Crowe Grade 2 or above, Perthes or other causes) Osteoporosis Paget's disease Inflammatory arthritis Secondary osteoarthritis Presence of malignancy in the area of surgery Treatment with bisphosphonates, cortisol or cytostatic drugs 6 months or less prior to surgery Previous surgery in the affected hip Inclusion of the contralateral hip in this clinical investigation Not suited for the clinical investigation for other reason (surgeon's judgment) Pregnant or breastfeeding women Prison inmate

Sites / Locations

  • Volker OttenRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

MobilLINK TrabecuLINK cup

Pinnacle Gription Series 100 cup

Arm Description

The investigational device in this study is the newly developed MobilLINK TrabecuLINK cup. It will in this study be combined with a uncemented LCU stem. The MobilLINK TrabecuLINK cups are made from Tilastan, a Ti6A4V alloy. The MobileLINK press-fit shells are hemispheric and polar flattened. An equatorial press-fit is built into the shells for primary stability after cementless implantation. All shells have a polar hole, which is used to connect an impactor handle for implantation of the shell. This polar hole can be closed with a polar screw. The MobileLINK TrabecuLINK shells have a 3D printed trabecular surface structure with a pore size of 610 to 820 μm and a porosity of 70 %.

For the control group a Pinnacle Gription cup series 100 with a apex hole eliminator will be used together with a neutral cross-linked polyethylene (XLPE) Marathon liner (DePuy Synthes by Johnson & Johnson, Norderstedt, Germany). The Pinnacle Gription cup is a hemispherical, single-geometry, titanium press-fit cup with a solid body. The outer surface consists of a porous coating with 300 μm sintered titanium beads coated with an extra layer of irregularly shaped pure titanium pieces. In cases where no initial stability can be reached when using the Pinnacle 100 series, the Pinnacle Gription sector cup with additional bone screws will be used. The cross-linked Marathon insert is made of 1050 GUR resin, irradiated with 50 kGy, remelted and plasma sterilized. The Pinnacle Gription cup will be implanted together with a Corail stem (DePuy Synthes).

Outcomes

Primary Outcome Measures

Early migration of the cup
Migration of the cup between 3 month and 2 years after implantation of the cup measured with Computed Tomography scan based Micromotion Analysis (CTMA) in mm.

Secondary Outcome Measures

Proximal wear
Liner wear measured as proximal penetration of the femoral head prosthesis into the liner between 1 year and 5 years after operation in mm
3D wear
Liner wear measured as 3D penetration of the femoral head prosthesis into the liner between 1 year and 5 years after operation in mm
Long term migratio
Migration of the cup measured in mm with CTMA
Long term wear
Liner wear measured in mm with CTMA
Stem migration
Distal and 3D migration in mm of the stem between post- operative examination and 3 month, 3 month and 2 years, 3 month and 5 years and 3 month and 15 years.
Patient reported outcome with Forgotten Joint Score
Patient-reported outcome measured by Forgotten Joint Score (FSJ). The scores will be summarized and transformed to a scale ranging from 0 to 100, where a high value indicate that the patient tends to be less aware of the affected joint when performing daily activities.
Patient reported outcome with Hip dysfunction and Osteoarthritis Outcome Score
Patient-reported outcome measured by Hip dysfunction and Osteoarthritis Outcome Score (HOOS). Each of the 5 subscales will get a score of 0 to 100, with 0 indicating extreme symptoms and 100 indicating no symptoms. The subscales will be plotted as a HOOS profile, by connecting the mean scores for all 5 dimensions with a line.
Patient reported outcome with University of California, Los Angeles Activity Score
Patient-reported outcome measured by University of California, Los Angeles Activity Score (UCLA). The patients physical activity level rank from 1 (low) to 10 (high).
Patient reported outcome with EuroQuol 5.
Patient reported health related quality of life, measured by EuroQuol 5 dimensions (EQ-5D). For the calculation of the EQ-5D index the standard value set version 2.1 for Sweden is used. Index scores range from 0 ( 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.
Reoperations
Incidence and rate of revisions, re-operations and operation-related complications
Osteolysis
Incidence and rate of patients showing osteolysis around the cup on CT scans and/or on x-rays
Precision of migration measurements with CTMA
Precision of migration measurement in mm with CTMA, by comparing double CT scans obtained on the same day at the 1 year follow-up.
Precision of wear mearurements with CTMA
Precision of wear measurement in mm with CTMA, by comparing double CT scans obtained on the same day at the 1 year follow-up.

Full Information

First Posted
November 21, 2022
Last Updated
March 6, 2023
Sponsor
Umeå University
Collaborators
University Hospital, Umeå, Region Västerbotten
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1. Study Identification

Unique Protocol Identification Number
NCT05773261
Brief Title
Clinical Investigation Comparing Two Different Ultra-porous Coated Surfaces of Uncemented Cups
Official Title
Modern Surfaces of the Uncemented Cup in Total Hip Arthroplasty: A Randomized, Clinical Investigation Comparing Two Different Ultra-porous Coated Surfaces of Uncemented Cups Using CT-based Micromotion Analysis and Clinical Evaluation
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 9, 2022 (Actual)
Primary Completion Date
September 9, 2026 (Anticipated)
Study Completion Date
September 9, 2039 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Umeå University
Collaborators
University Hospital, Umeå, Region Västerbotten

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
A randomised controlled study comparing two types of ultra-porous coated uncemented cups in total hip arthroplasty. Primary objective is to investigate if the clinical, radiological and patient-reported outcome of the new MobileLINK TabecuLINK cup combined with an X-LINKed insert is non-inferior to the clinical and radiological outcome of the Pinnacle Gription series 100 cup combined with the Marathon liner. Patients are evaluated up to 15 years postoperatively.
Detailed Description
The purpose of this study is to evaluate the clinical outcome and long-term risk of development of osteolysis of a newly introduced cementless press-fit acetabular cup, consisting of a shell with a 3D surface structure and a highly cross-linked liner by precise measurement of early migration and wear. Migration describes the movement between the implant and the surrounding bone over time. Early migration of the implant, within 2 years after operation, has shown to be a strong predictor for increased risk for late failure. Thus, high precision migration studies can be used to evaluate the performance of new implants in small groups of patients with a relatively short observation time. Wear particles are one of the main causes of periprosthetic osteolysis. Although modern, more wear resistant materials, appears to have a greatly reduced risk of osteolysis, the desired complete elimination of osteolysis appears to be yet unachieved. It is most likely that the mechanism of periprosthetic osteolysis is multifactorial. In this study the investigators plan to include 70 patients that are planned for operation with an uncemented total hip arthroplasty. 35 patients will be randomized to receive the new implant and 35 patients will be included in the control group and receive a standard uncemented prosthesis. All patients will then be followed with CT scans and patient reported outcome measures 3-month, 1 year, 2 years, 5 years and 15 years after the operations. The CT scans will be used both for measurement of migration and wear and development of osteolysis around the implant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Hip
Keywords
Osteoarthritis, Total hip arthroplasty, Uncemented total hip arthroplasty

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Control: Pinnacle Gription series 100 cup with a Marathon liner combined med with a Corail femoral stem. Investigational device: MobilLINK TrabecuLINK cup with X-LINKed liner combined with a LCU femoral stem.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MobilLINK TrabecuLINK cup
Arm Type
Active Comparator
Arm Description
The investigational device in this study is the newly developed MobilLINK TrabecuLINK cup. It will in this study be combined with a uncemented LCU stem. The MobilLINK TrabecuLINK cups are made from Tilastan, a Ti6A4V alloy. The MobileLINK press-fit shells are hemispheric and polar flattened. An equatorial press-fit is built into the shells for primary stability after cementless implantation. All shells have a polar hole, which is used to connect an impactor handle for implantation of the shell. This polar hole can be closed with a polar screw. The MobileLINK TrabecuLINK shells have a 3D printed trabecular surface structure with a pore size of 610 to 820 μm and a porosity of 70 %.
Arm Title
Pinnacle Gription Series 100 cup
Arm Type
Active Comparator
Arm Description
For the control group a Pinnacle Gription cup series 100 with a apex hole eliminator will be used together with a neutral cross-linked polyethylene (XLPE) Marathon liner (DePuy Synthes by Johnson & Johnson, Norderstedt, Germany). The Pinnacle Gription cup is a hemispherical, single-geometry, titanium press-fit cup with a solid body. The outer surface consists of a porous coating with 300 μm sintered titanium beads coated with an extra layer of irregularly shaped pure titanium pieces. In cases where no initial stability can be reached when using the Pinnacle 100 series, the Pinnacle Gription sector cup with additional bone screws will be used. The cross-linked Marathon insert is made of 1050 GUR resin, irradiated with 50 kGy, remelted and plasma sterilized. The Pinnacle Gription cup will be implanted together with a Corail stem (DePuy Synthes).
Intervention Type
Device
Intervention Name(s)
MobilLINK TrabecuLINK cup
Intervention Description
THA with MobilLINK TrabecuLINK cup and LCU stem
Intervention Type
Device
Intervention Name(s)
Pinnacle Gription cup
Intervention Description
THA with Pinnacle Gription cup and Coral stem
Primary Outcome Measure Information:
Title
Early migration of the cup
Description
Migration of the cup between 3 month and 2 years after implantation of the cup measured with Computed Tomography scan based Micromotion Analysis (CTMA) in mm.
Time Frame
2 years after operation
Secondary Outcome Measure Information:
Title
Proximal wear
Description
Liner wear measured as proximal penetration of the femoral head prosthesis into the liner between 1 year and 5 years after operation in mm
Time Frame
5 years after operation
Title
3D wear
Description
Liner wear measured as 3D penetration of the femoral head prosthesis into the liner between 1 year and 5 years after operation in mm
Time Frame
5 years after operation
Title
Long term migratio
Description
Migration of the cup measured in mm with CTMA
Time Frame
15 years after operation
Title
Long term wear
Description
Liner wear measured in mm with CTMA
Time Frame
15 years after operation
Title
Stem migration
Description
Distal and 3D migration in mm of the stem between post- operative examination and 3 month, 3 month and 2 years, 3 month and 5 years and 3 month and 15 years.
Time Frame
15 years
Title
Patient reported outcome with Forgotten Joint Score
Description
Patient-reported outcome measured by Forgotten Joint Score (FSJ). The scores will be summarized and transformed to a scale ranging from 0 to 100, where a high value indicate that the patient tends to be less aware of the affected joint when performing daily activities.
Time Frame
15 years after operation
Title
Patient reported outcome with Hip dysfunction and Osteoarthritis Outcome Score
Description
Patient-reported outcome measured by Hip dysfunction and Osteoarthritis Outcome Score (HOOS). Each of the 5 subscales will get a score of 0 to 100, with 0 indicating extreme symptoms and 100 indicating no symptoms. The subscales will be plotted as a HOOS profile, by connecting the mean scores for all 5 dimensions with a line.
Time Frame
15 years after operation
Title
Patient reported outcome with University of California, Los Angeles Activity Score
Description
Patient-reported outcome measured by University of California, Los Angeles Activity Score (UCLA). The patients physical activity level rank from 1 (low) to 10 (high).
Time Frame
15 years after operation
Title
Patient reported outcome with EuroQuol 5.
Description
Patient reported health related quality of life, measured by EuroQuol 5 dimensions (EQ-5D). For the calculation of the EQ-5D index the standard value set version 2.1 for Sweden is used. Index scores range from 0 ( 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.
Time Frame
15 years after operation
Title
Reoperations
Description
Incidence and rate of revisions, re-operations and operation-related complications
Time Frame
15 years after operation
Title
Osteolysis
Description
Incidence and rate of patients showing osteolysis around the cup on CT scans and/or on x-rays
Time Frame
15 years after operation
Title
Precision of migration measurements with CTMA
Description
Precision of migration measurement in mm with CTMA, by comparing double CT scans obtained on the same day at the 1 year follow-up.
Time Frame
1 year after operation
Title
Precision of wear mearurements with CTMA
Description
Precision of wear measurement in mm with CTMA, by comparing double CT scans obtained on the same day at the 1 year follow-up.
Time Frame
1 year after operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients are foreseen for implantation of an uncemented acetabular press-fit cup and an uncemented stem Age 30-70 years Primary osteoarthritis of the hip Body Mass Index between 18 and 35 kg/m2 Willingness and ability to follow clinical investigation protocol Exclusion Criteria: Grossly abnormal hip anatomy (hip dysplasia, Crowe Grade 2 or above, Perthes or other causes) Osteoporosis Paget's disease Inflammatory arthritis Secondary osteoarthritis Presence of malignancy in the area of surgery Treatment with bisphosphonates, cortisol or cytostatic drugs 6 months or less prior to surgery Previous surgery in the affected hip Inclusion of the contralateral hip in this clinical investigation Not suited for the clinical investigation for other reason (surgeon's judgment) Pregnant or breastfeeding women Prison inmate
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Volker TC Otten, Ph.D
Phone
0046907850000
Email
volker.otten@umu.se
First Name & Middle Initial & Last Name or Official Title & Degree
Sebastian Mukka, Ph.D
Email
sebastian.mukka@umu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Volker Otten, M.D, PhD
Organizational Affiliation
Umeå University hospital/Umeå University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Volker Otten
City
Umeå
State/Province
Västerbotten
ZIP/Postal Code
907 37
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Volker TC Otten, Ph.D
Phone
+46703341558
Email
volker.otten@regionvasterbotten.se
First Name & Middle Initial & Last Name & Degree
Sebastian Mukka, Ph.D
Email
sebastian.mukka@umu.se
First Name & Middle Initial & Last Name & Degree
Volker TC Otten, Ph.D
First Name & Middle Initial & Last Name & Degree
Sebastian Mukka, Ph.D
First Name & Middle Initial & Last Name & Degree
Daniel Wästerlund, M.D.
First Name & Middle Initial & Last Name & Degree
Krenare Mehmeti, Medical student

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29092981
Citation
Buttaro MA, Onativia JI, Slullitel PA, Andreoli M, Comba F, Zanotti G, Piccaluga F. Metaphyseal debonding of the Corail collarless cementless stem: report of 18 cases and case-control study. Bone Joint J. 2017 Nov;99-B(11):1435-1441. doi: 10.1302/0301-620X.99B11.BJJ-2017-0431.R1. Erratum In: Bone Joint J. 2018 Sep;100-B(9):1260. Bone Joint J. 2018 Sep;100-B(9):1260.
Results Reference
background
PubMed Identifier
28778624
Citation
Louboutin L, Viste A, Desmarchelier R, Fessy MH. Long-term survivorship of the Corail standard stem. Orthop Traumatol Surg Res. 2017 Nov;103(7):987-992. doi: 10.1016/j.otsr.2017.06.010. Epub 2017 Aug 1.
Results Reference
background
PubMed Identifier
25909455
Citation
van der Voort P, Pijls BG, Nieuwenhuijse MJ, Jasper J, Fiocco M, Plevier JW, Middeldorp S, Valstar ER, Nelissen RG. Early subsidence of shape-closed hip arthroplasty stems is associated with late revision. A systematic review and meta-analysis of 24 RSA studies and 56 survival studies. Acta Orthop. 2015;86(5):575-85. doi: 10.3109/17453674.2015.1043832.
Results Reference
background
PubMed Identifier
18594097
Citation
Bitsch RG, Loidolt T, Heisel C, Ball S, Schmalzried TP. Reduction of osteolysis with use of Marathon cross-linked polyethylene. A concise follow-up, at a minimum of five years, of a previous report. J Bone Joint Surg Am. 2008 Jul;90(7):1487-91. doi: 10.2106/JBJS.F.00991.
Results Reference
background
PubMed Identifier
20012862
Citation
Campbell D, Mercer G, Nilsson KG, Wells V, Field JR, Callary SA. Early migration characteristics of a hydroxyapatite-coated femoral stem: an RSA study. Int Orthop. 2011 Apr;35(4):483-8. doi: 10.1007/s00264-009-0913-z. Epub 2009 Dec 13.
Results Reference
background
PubMed Identifier
24269067
Citation
Goriainov V, Jones A, Briscoe A, New A, Dunlop D. Do the cup surface properties influence the initial stability? J Arthroplasty. 2014 Apr;29(4):757-62. doi: 10.1016/j.arth.2013.07.007. Epub 2013 Nov 22.
Results Reference
background
PubMed Identifier
23510822
Citation
Drobniewski M, Borowski A, Synder M, Sibinski M. Results of total cementless hip joint arthroplasty with Corail stem. Ortop Traumatol Rehabil. 2013 Jan-Feb;15(1):61-8. doi: 10.5604/15093492.1032797.
Results Reference
background

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Clinical Investigation Comparing Two Different Ultra-porous Coated Surfaces of Uncemented Cups

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