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Antibiotic Loaded Bone Cement in Prevention of Periprosthetic Joint Infections in Primary Total Knee Arthroplasty (ALBA)

Primary Purpose

Osteoarthritis, Knee

Status
Recruiting
Phase
Phase 2
Locations
Norway
Study Type
Interventional
Intervention
ALBC vs plain bone cement
Sponsored by
The Norwegian Arthroplasty Register
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Osteoarthritis, Knee focused on measuring Register based randomized control trial, Non-inferiority, Total knee arthroplasty, Antibiotic loaded bone cement, Plain bone cement, Antibiotic resistance bacteria, Periprosthetic joint infection, Patient reported outcome measure, Health related quality of life, Pain, Function, Satisfaction, Revision surgery, Primary surgery

Eligibility Criteria

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

Inclusion Criteria:

  • all patients undergoing full-cemented primary TKA irrespective of the diagnosis leading to TKA

Exclusion Criteria:

  • any history of infection in the knee, a need for fully stabilized or hinged TKA, a history of allergy to the antibiotics used in the cement, inability or not willing to consent for inclusion in NAR or the trial, and participation in other studies that might have pharmacological interaction with this trial.

Sites / Locations

  • Department of Orthopeadic Surgery, Haukeland University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Plain bone cement

Antibiotic loaded bone cement

Arm Description

Outcomes

Primary Outcome Measures

risk of revision due to PJI

Secondary Outcome Measures

risk of revision due to any reason including aseptic loosening
risk of changes in the microbial pattern and resistance profiles of organisms cultured in subsequent revisions
Change in mean scores from baseline function (in activity of daily life) on the Knee injury and Osteoarthritis Outcome Score (KOOS).
Change in mean scores from baselinein in Visual Analog Sale (the scores range from 0 to 100, with 0 indicating the worst possible state and 100 indicating the best possible state) for pain.
Change in mean scores from baseline in EQ-5D-5L for health related quality of life(HRQoL).
Mean scores in Visual Analog Sale ( the scores range from 0 to 100, with 0 indicating the worst possible state and 100 indicating the best possible state) for patient satisfaction.

Full Information

First Posted
September 20, 2019
Last Updated
January 14, 2021
Sponsor
The Norwegian Arthroplasty Register
Collaborators
Helse Vest
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1. Study Identification

Unique Protocol Identification Number
NCT04135170
Brief Title
Antibiotic Loaded Bone Cement in Prevention of Periprosthetic Joint Infections in Primary Total Knee Arthroplasty
Acronym
ALBA
Official Title
Antibiotic Loaded Bone Cement in Prevention of Periprosthetic Joint Infections in Primary Total Knee Arthroplasty: A Register-based Multicenter Randomized Controlled Non-inferiority Trial (Acronym: ALBA Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Recruiting
Study Start Date
January 14, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Norwegian Arthroplasty Register
Collaborators
Helse Vest

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Introduction: The current evidence on the efficacy of Antibiotic Loaded Bone Cement (ALBC) in reducing the risk of periprosthetic joint infections (PJI) after primary joint reconstruction is insufficient. In several European countries, the use of ALBC is routine practice unlike in the US where ALBC use is not approved in low-risk patients. It has been claimed that the antibiotic in ALBC increase the risk of aseptic loosening, risk of systemic toxicity, allergic reaction, and bacterial resistance. Therefore we designed a double-blinded (patients and data analysts) pragmatic multicenter register-based randomized controlled non-inferiority trial to investigate the effects of ALBC compared to plain bone cement in primary total knee arthroplasty (TKA). Methods and analysis: A minimum of 9,172 patients undergoing full-cemented primary TKA will be recruited and equally randomized into the ALBC group and the plain bone cement group. This trial will be conducted in Norwegian hospitals that routinely perform cemented primary TKA. . The primary outcome will be risk of revision surgery due to PJI at 1-year of follow-up. Secondary outcomes will be: risk of revision due to any reason including aseptic loosening at 1-, 6-, 10-, and 20-years of follow-up; patient related outcome measures (PROMs) like function, pain, satisfaction, and health-related quality of life at 1-, 6-, and 10-years of follow-up; risk of changes in the microbial pattern and resistance profiles of organisms cultured in subsequent revisions at 1-, 6-, 10-, and 20-years of follow-up; and cost-effectiveness of routine ALBC vs plain bone cement use in primary TKA. We will use 1:1 randomization with random permuted blocks and stratify by participating hospitals to randomize patients to receive ALBC or plain bone cement. Inclusion, randomization, and follow-up will be through the Norwegian Arthroplasty Register. Ethics and dissemination: The trial has been approved by the Western Norway Regional Committees on Medical and Health Research Ethics (REK-Vest) (reference number: 2019/751/REK vest) dated: 21.06.2019. The trial results will be reported following the Consolidated Standards of Reporting Trials Extension (CONSORT Extension) reporting guideline 2010 statement for non-inferiority trials. The trial results will be reported to the public through national and international scientific conferences, participating hospitals, patient organizations, and peer-reviewed journals. Discussion: If we find that plain bone cement is non-inferior to the ALBC, it will challenge the routine use of ALBC in primary arthroplasty, due to ecological concerns and costs. However, if routine use of ALBC is associated with a reduced risk of PJI and with minor impact on bacterial resistance, PROMs, and costs, the well-established use of prophylactic ALBC in primary arthroplasty will be supported

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
Keywords
Register based randomized control trial, Non-inferiority, Total knee arthroplasty, Antibiotic loaded bone cement, Plain bone cement, Antibiotic resistance bacteria, Periprosthetic joint infection, Patient reported outcome measure, Health related quality of life, Pain, Function, Satisfaction, Revision surgery, Primary surgery

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Patients undergoing full-cemented primary TKA in any Norwegian hospitals are eligible for participation irrespectively of the diagnosis leading to TKA. and randomly assigned to receive ALBC (control group) or plain bone cement (experimental group).
Masking
ParticipantOutcomes Assessor
Masking Description
This is a double blinded, non-inferiority register-based multicenter randomized controlled trial study. To ensure blinding of the patients, all patients are operated by the same surgical method and the type of cement is unknown to the patients. In this study, blinding of the surgeon is not possible because the surgeon recognizes the cement type and has to document the type of cement in the registration form. We believe the primary endpoint of this trial is not likely to be influenced by the surgeon knowledge of the cement used in the index surgery. The data analyst will be blinded for groups until the entire trial analysis has been completed to minimize the risk of bias that may be introduced during the statistical analysis because of the selective use and reporting of statistical tests.
Allocation
Randomized
Enrollment
9172 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Plain bone cement
Arm Type
Experimental
Arm Title
Antibiotic loaded bone cement
Arm Type
Active Comparator
Intervention Type
Combination Product
Intervention Name(s)
ALBC vs plain bone cement
Intervention Description
The patients undergoing full-cemented primary total knee arthroplasty are allocated to either ALBC or plain bone cement and compare the effectiveness of ALBC use vs pain bone cement bone cement without antibiotic) with respect to revision due to PJI one year after primary TKA surgery.
Primary Outcome Measure Information:
Title
risk of revision due to PJI
Time Frame
1-year follow-up
Secondary Outcome Measure Information:
Title
risk of revision due to any reason including aseptic loosening
Time Frame
1-, 6-, 10-, and 20-years follow-up
Title
risk of changes in the microbial pattern and resistance profiles of organisms cultured in subsequent revisions
Time Frame
1-, 6-, 10-, and 20-years follow-up
Title
Change in mean scores from baseline function (in activity of daily life) on the Knee injury and Osteoarthritis Outcome Score (KOOS).
Time Frame
1-, 6-, and 10-years follow-up
Title
Change in mean scores from baselinein in Visual Analog Sale (the scores range from 0 to 100, with 0 indicating the worst possible state and 100 indicating the best possible state) for pain.
Time Frame
1-, 6-, and 10-years follow-up
Title
Change in mean scores from baseline in EQ-5D-5L for health related quality of life(HRQoL).
Time Frame
1-, 6-, and 10-years follow-up
Title
Mean scores in Visual Analog Sale ( the scores range from 0 to 100, with 0 indicating the worst possible state and 100 indicating the best possible state) for patient satisfaction.
Time Frame
1-, 6-, and 10-years follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: all patients undergoing full-cemented primary TKA irrespective of the diagnosis leading to TKA Exclusion Criteria: any history of infection in the knee, a need for fully stabilized or hinged TKA, a history of allergy to the antibiotics used in the cement, inability or not willing to consent for inclusion in NAR or the trial, and participation in other studies that might have pharmacological interaction with this trial.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tesfaye H Leta, PhD
Phone
+4791691925
Email
tesfaye.hordofa.leta@helse-bergen.no
First Name & Middle Initial & Last Name or Official Title & Degree
Ove Furnes, MD/PhD
Phone
+4790840088
Email
ove.nord.furnes@helse-bergen.no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ove Furnes, MD/PhD
Organizational Affiliation
The Norwegian Arthroplasty Register, Department of Orthopedic Surgery, Haukeland University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Orthopeadic Surgery, Haukeland University Hospital
City
Bergen
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ove Furnes, PhD
Phone
55975690
Ext
0047
Email
ove.nord.furnes@helse-bergen.no

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33509845
Citation
Leta TH, Gjertsen JE, Dale H, Hallan G, Lygre SHL, Fenstad AM, Dyrhovden GS, Westberg M, Wik TS, Jakobsen RB, Aamodt A, Rohrl SM, Gothesen OJ, Lindalen E, Heir S, Ludvigsen J, Bruun T, Hansen AK, Aune KEM, Warholm M, Skjetne JP, Badawy M, Hovding P, Husby OS, Karlsen OE, Furnes O. Antibiotic-Loaded Bone Cement in Prevention of Periprosthetic Joint Infections in Primary Total Knee Arthroplasty: A Register-based Multicentre Randomised Controlled Non-inferiority Trial (ALBA trial). BMJ Open. 2021 Jan 28;11(1):e041096. doi: 10.1136/bmjopen-2020-041096.
Results Reference
derived

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Antibiotic Loaded Bone Cement in Prevention of Periprosthetic Joint Infections in Primary Total Knee Arthroplasty

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