Sigma CR150 Versus Sigma CR Knee RCT

Osteoarthritis Clinical Trial

Official title:

A Double-blinded Randomised Controlled Trial Comparing the Performance of the Sigma® CR150 and Sigma® CR Knee Systems, When Used in Fixed Bearing Primary Cruciate Retaining Total Knee Arthroplasty for the Treatment of Osteoarthritis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01418378
• Other study ID #: CT07/04
• Status: Completed
• Phase: Phase 4
• Start date: August 3, 2011
• Est. completion date: February 17, 2016

Study information

• Verified date: July 2019
• Source: DePuy International
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will compare two very similar designs of knee replacement device. One device (Sigma CR150) is a slightly modified version of the original (Sigma CR) and has been modified to enhance/accommodate higher flexion. The original device has been in widespread clinical use with excellent results since 1996 and this study will determine whether the design modifications of the newer device add further value. The newer device has been in clinical use with good short-term(unpublished) outcomes since becoming commercially available in January 2009.

Achieving higher knee flexion may be required for cultural reasons or by the increasingly younger, more active patient population undergoing knee replacement today. In addition to promoting flexion, it is also possible that this design change may help the knee replacement to last longer than traditional implants in patients who achieve higher flexion. Therefore, the study will compare the two devices in terms of survivorship, flexion and other measures of the success of a total knee replacement (range of motion, knee-related quality of life, activity and generic quality of life) over the short-term.

A minimum of one hundred and forty subjects (minimum 70 per group) with osteoarthritis and aged 50-75 years will be included at UK/international hospitals.

Study duration is 2 years and patients will complete standard knee outcome scores plus radiological evaluation.

Subjects would receive one of the study devices regardless of their involvement in the study, and apart from (possible)additional visits, x-rays and/or questionnaires, treatment and follow-up care will be as per the care they would receive outside of the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 191
• Est. completion date: February 17, 2016
• Est. primary completion date: February 17, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 50 Years to 75 Years

Eligibility

Inclusion Criteria:

i)Male or female subjects, aged between 50 and 75 years inclusive.

ii)Subjects who are able to give voluntary, written informed consent to participate in this clinical investigation and from whom consent has been obtained.

iii) Subjects who, in the opinion of the Clinical Investigator, are able to understand this clinical investigation, co-operate with the investigational procedures and are willing to return to the hospital for all the required post-operative follow-ups.

iv) Subjects defined by the Investigator as ASA Grade I or II.

v) Subjects with a primary diagnosis of osteoarthritis.

vi) Subjects who require a primary total knee arthroplasty.

vii) Subjects who can achieve active flexion of 90 degrees.

Exclusion Criteria:

i) Subjects who, in the opinion of the Clinical Investigator, have an existing condition that would compromise their participation and follow-up in this clinical investigation.

ii) Subjects who are known drug or alcohol abusers or with psychological disorders that could affect follow-up care or treatment outcomes.

iii) Subjects who have participated in a clinical investigation with an investigational product in the last month.

iv) Subjects who are currently involved in any injury litigation claims.

v) Subjects with an anatomical limb alignment of above 20 degrees varus or valgus.

vi) Subjects with a fixed flexion deformity of over 20 degrees.

vii) Subjects with recurvatum (definition: hyperextension = 5 degrees).

viii) Subjects who cannot flex their hip to 90 degrees.

ix) Subjects with a BMI of 35 or above.

x) Subjects defined by the Investigator as ASA Grade III-V.

xi) Subjects who are identified pre-operatively as having bone defects which require augmentation.

xii) Subjects who have previously undergone total or unicondylar knee arthroplasty, high tibial osteotomy, ligament reconstruction, ORIF or with previous fracture in the knee joint.

xiii) Subjects with primary or secondary diagnosis of inflammatory or traumatic arthritis.

xiv) Subjects who have undergone contralateral total knee arthroplasty during the previous 6 months.

xv) Subjects who in the opinion of the Investigator require patellar resurfacing.

Intra-operative exclusion criteria:

i) Subjects who have uncontained bone defects or defects bigger than 8 mm3 and/or require augmentation.

ii) Subjects who are not suitable to receive both the study and comparator devices.

iii) Subjects who require patellar resurfacing

Related Conditions & MeSH terms

• Osteoarthritis

Intervention

Device:
• Sigma CR150
Sigma CR150 femoral component used in combination with the Highly Polished Cobalt Chrome fixed bearing tibial tray and the Curved (XLK) polyethylene bearing (cemented, no patellar resurfacing).
• Sigma CR
Sigma CR femoral component used in combination with the Highly Polished Cobalt Chrome fixed bearing tibial tray and the Curved (XLK) polyethylene bearing (cemented, no patellar resurfacing).

Locations

Country	Name	City	State
India	Sunshine Hospitals	Secunderabad	Andhra Pradesh
Singapore	Singapore General Hospital	Singapore
United Kingdom	Calderdale Royal Hospital	Halifax	West Yorkshire
United Kingdom	Victoria Hospital	Kirkcaldy	Fife

Sponsors (1)

Lead Sponsor	Collaborator
DePuy International

Countries where clinical trial is conducted

India,  Singapore,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of Knees Who Survived at 2 Years Post-operative	The Kaplan-Meier success rate at 24-months post-operatively was calculated with Kaplan-Meier time-to-event methodology, where the time variable for patients who were successful (no components revised for any reason) was censored at the time of last follow-up.	2 Years
Secondary	Change From Baseline in Goniometer Measured Maximum Passive Flexion at 2 Years	Comparative evaluation of the change from baseline values in 2 year goniometer-measured passive flexion. A goniometer is an instrument used to measure angles in degrees and captures the change in angle between the upper and lower leg	Pre-operative baseline to 2 years
Secondary	Knee Injury and Osteoarthritis Outcome Pain Subscore - 1 Year	Comparative evaluation of the change from baseline values at 1 years in Knee Injury and Osteoarthritis Outcome Pain Subscore; The subscore ranges from 0 (no pain) to 36 (extreme pain). The subscore is then transformed into a 0 (extreme pain) to 100 (no pain) scale.; 100 - (score x 100) / 36 = transformed score	Pre-operative baseline to 1 year
Secondary	Knee Injury and Osteoarthritis Outcome Pain Subscore - 2 Years	Comparative evaluation of the change from baseline values at 2 years in Knee Injury and Osteoarthritis Outcome Pain Subscore; The subscore ranges from 0 (no pain) to 36 (extreme pain). The subscore is then transformed into a 0 (extreme pain) to 100 (no pain) scale.; 100 - (score x 100) / 36 = transformed score	2 years
Secondary	Knee Injury and Osteoarthritis Outcome Symptoms Subscore - 1 Years	Comparative evaluation of the change from baseline values at 1 year in Knee Injury and Osteoarthritis Outcome Symptom Subscore; The subscore ranges from 0 (no symptoms) to 36 (always have symptoms). The subscore is then transformed into a 0 (always have symptoms) to 100 (never have symptoms) scale.; 100 - (score x 100) / 36 = transformed score	1 years
Secondary	Knee Injury and Osteoarthritis Outcome Symptom Subscore - 2 Years	Comparative evaluation of the change from baseline values at 2 years in Knee Injury and Osteoarthritis Outcome Symptom Subscore; The subscore ranges from 0 (never have symptoms) to 28 (always have symptoms). The subscore is then transformed into a 0 (always have symptoms) to 100 (never have symptoms) scale.; 100 - (score x 100) / 28 = transformed score	2 years
Secondary	Knee Injury and Osteoarthritis Outcome - Activities of Daily Living Subscore - 1 Years	Comparative evaluation of the change from baseline values at 1 years in Knee Injury and Osteoarthritis Outcome Symptom Subscore; The subscore ranges from 0 (no difficulty) to 68 (extreme difficulty). The subscore is then transformed into a 0 (extreme difficulty) to 100 (no difficulty) scale.; 100 - (score x 100) / 68 = transformed score	1 year
Secondary	Knee Injury and Osteoarthritis Outcome - Activities of Daily Living Subscore - 2 Years	Comparative evaluation of the change from baseline values at 2 years in Knee Injury and Osteoarthritis Outcome Activities of Daily Living Subscore; The subscore ranges from 0 (no difficulty) to 68 (extreme difficulty). The subscore is then transformed into a 0 (extreme difficulty) to 100 (no difficulty) scale.; 100 - (score x 100) / 68 = transformed score	2 year
Secondary	Knee Injury and Osteoarthritis Outcome - Sport and Recreation Subscore - 1 Years	Comparative evaluation of the change from baseline values at 1 years in Knee Injury and Osteoarthritis Outcome Activities of Daily Living Subscore; The subscore ranges from 0 (no difficulty) to 20 (extreme difficulty). The subscore is then transformed into a 0 (extreme difficulty) to 100 (no difficulty) scale.; 100 - (score x 100) / 20 = transformed score	1 year
Secondary	Knee Injury and Osteoarthritis Outcome Sport and Recreation Subscore - 2 Years	Comparative evaluation of the change from baseline values at 2 years in Knee Injury and Osteoarthritis Outcome Activities of Daily Living Subscore; The subscore ranges from 0 (no difficulty) to 20 (extreme difficulty). The subscore is then transformed into a 0 (extreme difficulty) to 100 (no difficulty) scale.; 100 - (score x 100) / 20 = transformed score	2 year
Secondary	Knee Injury and Osteoarthritis Outcome - Quality of Life Subscore - 1 Years	Comparative evaluation of the change from baseline values at 1 years in Knee Injury and Osteoarthritis Outcome Activities of Quality of life Subscore; The subscore ranges from 0 (no difficulty) to 16 (extreme difficulty). The subscore is then transformed into a 0 (extreme difficulty) to 100 (no difficulty) scale.; 100 - (score x 100) / 16 = transformed score	1 year
Secondary	Knee Injury and Osteoarthritis Outcome - Quality of Life Subscore - 2 Years	Comparative evaluation of the change from baseline values at 2 years in Knee Injury and Osteoarthritis Outcome Quality of Life Subscore; The subscore ranges from 0 (no difficulty) to 16 (extreme difficulty). The subscore is then transformed into a 0 (extreme difficulty) to 100 (no difficulty) scale.; 100 - (score x 100) / 16 = transformed score	2 years
Secondary	Change From Baseline in Goniometer Measured Maximum Passive Flexion at 1 Year.	Comparative evaluation of the change from baseline values in 1 year goniometer-measured passive Flexion. A goniometer is an instrument used to measure angles in degrees and captures the change in angle between the upper and lower leg. Passive flexion involves moving the leg through range of motion without active muscle contraction	1 year
Secondary	Change From Baseline in Goniometer Measured Maximum Passive Extension at 1 Year	Comparative evaluation of the change from baseline values in 1 year goniometer-measured passive extension. A goniometer is an instrument used to measure angles in degrees and captures the change in angle between the upper and lower leg. Passive extension involves the leg being moved without active muscle contraction	1 year
Secondary	Change From Baseline in Goniometer Measured Maximum Passive Extension at 2 Years	Comparative evaluation of the change from baseline values in 2 year goniometer-measured passive extension. A goniometer is an instrument used to measure angles in degrees and captures the change in angle between the upper and lower leg. Passive extension involves moving the leg without active muscle contraction	2 year
Secondary	Change From Baseline in Goniometer Measured Maximum Total Range of Motion at 1 Year	Comparative evaluation of the change from baseline values in 1 year goniometer-measured total range of motion. A goniometer is an instrument used to measure angles in degrees and captures the change in angle between the upper and lower leg. Total range of motion is the full distance the lower leg travels in relation to the upper leg.	1 year
Secondary	Change From Baseline in Goniometer Measured Maximum Total Range of Motion at 2 Years.	Comparative evaluation of the change from baseline values in 2 year goniometer-measured total range of motion. A goniometer is an instrument used to measure angles in degrees and captures the change in angle between the upper and lower leg. Total range of motion is the full distance the lower leg travels in relation to the upper leg.	2 years
Secondary	Number of Participants With Flexion Contracture at 1 Year	Summary of flexion contracture at 1 year time point. Flexion contracture is a shortening of the muscles that prevents the leg from fully extending	1 years
Secondary	Number of Participants With Flexion Contracture at 2 Years	Summary of flexion contracture at 2 year time point.Flexion contracture is a shortening of the muscles that prevents the leg from fully extending	2 years
Secondary	Total Knee Society Score at 1 Year	Total Knee Society Knee Score change from baseline at 1 year; The Total Knee Society Score is comprised of two scores: the Knee Score and the Function Score. Both have a 0-100 range. Sub-scales are combined to compute a total score of 100; The Total Knee Society Score is made up of pain, range of motion, alignment and stability subscores. An Excellent score is 80-100, a good score is 70-79, a fair score is 60-69 and a poor score is anything below 60.	1 year
Secondary	Total Knee Society Knee Score at 2 Years	Total Knee Society Knee Score change from baseline at 2 years; The Total Knee Society Score is comprised of two scores: the Knee Score and the Function Score. Both have a 0-100 range. Sub-scales are combined to compute a total score of 100; The Total Knee Society Score is made up of pain, range of motion, alignment and stability subscores. An Excellent score is 80-100, a good score is 70-79, a fair score is 60-69 and a poor score is anything below 60.	2 years
Secondary	Anatomic Alignment Angle	Anatomic angle measured at 1 year time point.; If one draws a line from the center of the hip joint to the center of the ankle joint this is considered to be the mechanical axis of the femur.; A line drawn through the center of the femoral shaft is the anatomic axis.; The angle created at the intersection of these lines is referred to as the anatomic alignment angle.; A normal angle is approximately 7-9 degrees "valgus" or slightly "knock-kneed". "Varus" angles are less common and are also referred to as "bow-legged".	1 year time point
Secondary	Anatomic Alignment Angle	Anatomic angle measured at 2 year time point.; If one draws a line from the center of the hip joint to the center of the ankle joint this is considered to be the mechanical axis of the femur.; A line drawn through the center of the femoral shaft is the anatomic axis.; The angle created at the intersection of these lines is referred to as the anatomic alignment angle.; A normal angle is approximately 7-9 degrees "valgus" or slightly "knock-kneed". "Varus" angles are less common and are also referred to as "bow-legged".	2 year time point
Secondary	Alignment - Femoral Component to Anatomic Angle.	Femoral component angle measured at 1 year time point. This angle is measured between a line drawn from the center of the femoral head and a line across the bottom of the femoral implant (condyles).	1 year time point
Secondary	Alignment - Femoral Component to Anatomic Angle	Femoral component angle measured at 2 year time point. This angle is measured between a line drawn from the center of the femoral head and a line across the bottom of the femoral implant (condyles).	2 year time point
Secondary	Alignment - Tibial Component to Anatomic Angle	Tibial component angle measured at 1 year time point. This angle is measured between a line drawn from the center of the femoral head tibial implant.	1 year time point
Secondary	Alignment - Tibial Component to Anatomic Angle	Tibial component angle measured at 2 year time point. This angle is measured between a line drawn from the center of the femoral head tibial implant.	2 year time point
Secondary	Alignment - Femoral Component Flexion	Femoral Component Flexion measured at 1 year time point. This measures the angle between a line drawn though the center of the side of the femur and a line drawn across the top of the flat inner surface of the femoral component.	1 year time point
Secondary	Alignment - Femoral Component Flexion	Alignment - Femoral Component Flexion measured at 2 year time point. This measures the angle between a line drawn though the center of the side of the femur and a line drawn across the top of the flat inner surface of the femoral component.	2 year time point
Secondary	Alignment - Tibial Posterior Slope	Tibial Posterior Slope measured at 1 year time point. This angle is measured between a line through the center of the side of the tibia and the top flat surface of the tibial implant	1 year time point
Secondary	Alignment - Tibial Posterior Slope	Alignment - Tibial Posterior Slope measured at 2 year time point. This angle is measured between a line through the center of the side of the tibia and the top flat surface of the tibial implant	2 year time point
Secondary	Number of Subjects With Radiolucencies - Femoral Component	The bone-implant interface at the femoral components were examined radiographically and radiolucencies were measured in millimeters.; Radiolucent lines (RLLs) greater than 2mm are considered to be clinically significant.	6 to 12 week and 24 month intervals
Secondary	Number of Subjects With Radiolucencies - Tibial Component	The bone-implant interface at the tibial components were examined radiographically and radiolucencies were measured in millimeters.; Radiolucent lines (RLLs) greater than 2mm are considered to be clinically significant.; Radiolucent lines greater than 2mm are considered to be clinically significant.	6 weeks to 24 months
Secondary	Radiographic Evaluation of Maximum Flexion	Maximum knee flexion measured radiographically at 1 year time point	1 year time point