Unity Total Knee Replacement Using Two Different Surgical Techniques

Arthritis of the Knee Clinical Trial

Official title:

Unity Total Knee Replacement: Prospective Single-centre Clinical Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02145455
• Other study ID #: CSP2013-08
• Status: Completed
• Phase: N/A
• Start date: June 6, 2015
• Est. completion date: May 2020

Study information

• Verified date: July 2020
• Source: Corin
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will compare two different surgical methods used in total knee replacement with the Unity Total Knee Replacement System. The study will evaluate these two methods based on patients' ability to perform various tasks prior to surgery and at 4 time points during the first 12 months after surgery.

Description:

This study will be conducted at a single centre. The study has two treatment groups. One group of 50 knees (approximately 50 subjects) will have a surgical method that uses mechanical alignment (alignment based on how the leg and knee joint move) to determine the proper position of the knee replacement device. The other group of 50 knees (approximately 50 subjects) will have a surgical method that uses anatomical alignment (alignment based on how the anatomy/structure of the leg and knee joint) determine the proper position of the knee replacement device. Subjects will be randomly assigned to one of the two groups. Clinical and functional tests will be conducted pre-operatively and at 6 weeks, 3 months, 6 months and 12 months to determine overall knee function. In addition, a CT scan will be completed pre-operatively and at 6 weeks to assess changes in alignment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 111
• Est. completion date: May 2020
• Est. primary completion date: May 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• The patient must be listed for a primary total knee replacement using the Corin Unity Total Knee Replacement System, according to the product 'Instructions For Use'

• The patient must give signed informed consent to participate in the study

• The patient must be able to understand all that is expected of them and be able to comply with the study protocol

• Male and female patients who are skeletally mature

Exclusion Criteria:

• Any patient with a total knee replacement not implanted with a Corin Unity Total Knee Replacement

• Any patient with a revision total knee replacement or conversion of a Unicondylar replacement to a total knee replacement on the operative knee

• Any patient with fixed flexion contracture greater than 20 degrees

• Any patient with varus/valgus deformity greater than 15 degrees

• Any case not described in the inclusion criteria

• Any patient who cannot or will not provide signed informed consent for participation in the study

• Any patient whose prospects for a recovery to independent mobility would be compromised by known co-existent, medical problems

• Any patient with a known sensitivity to device material

• Any patient who is pregnant

• Any patient currently a prisoner

• Any patient known to be a drug or alcohol abuser, or have a psychological disorder that could affect follow-up care or treatment outcomes

• Any patient currently involved in any personal injury litigation, medical-legal or worker's compensations claims

• Any patient unable to read and understand English

Related Conditions & MeSH terms

• Arthritis
• Arthritis of the Knee

Intervention

Device:
• Unity Total Knee Replacement System

• Unity Total Knee Replacement System

Locations

Country	Name	City	State
United Kingdom	Exeter Knee Reconstruction Unit at the Princess Elizabeth Orthopaedic Centre	Exeter	Devon

Sponsors (1)

Lead Sponsor	Collaborator
Corin

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Power of knee extension	Power of knee extension via peak torque of quads measured on a digital myometer.	12 months post-operative
Secondary	Timed up and go test	The test measures the length of time it takes the subject to rise from a chair, walk 10 feet, turn around, and sit back down in the chair. The subject may rest or use walking aids during the test.	12 months post-operative
Secondary	Single leg stance (SLS) test	The test measures the length of time the subject can stand on their operative leg.	12 months post-operative
Secondary	6 minute walk test	The test measures the length of distance a subject can walk in 6 minutes at a pace that does not cause them to become short of breath. Patient may stop and rest if needed, then resume.	12 months post-operative
Secondary	Timed stairs test	The test measures the length of time it takes a subject to climb up a stair block and down the other side. The subject is asked how difficult the test was on a scale of 0 to 10. The subject can use the rails, if needed.	12 months post-operative
Secondary	Wii Fit balance test	The subject is asked to stand on a Wii Fit balance board while the "Deep breathing" exercise in the Yoga section is selected. The subject is instructed to follow the instructions on the screen. The subject's score is recorded and the subject is asked how difficult the test was on a scale from 1 to 10.	12 months post-operative
Secondary	Ability to kneel	The subject is asked to kneel on a mat on the floor and then rise to a standing position. The subject may use a bench or the floor for balance. After the test, the subject is asked how difficult the test was on a scale of 1 to 10. The subject is allowed to refuse to do the test if he/she feels unable to do so.	12 months post-operative
Secondary	Sloped treadmill test	The subject is asked to walk on a level treadmill at a comfortable walking speed. The incline of the treadmill is increased until the subject says stop or the limit of the treadmill is reached. The test is repeated with the treadmill in reverse and the subject facing backwards to simulate walking downhill. The subject is asked how difficult the test was on a scale of 1 to 10.	12 months post-operative
Secondary	Walking on uneven ground	The subject is asked to walk from one end to the other on a specialized track topped with fist-sized pebbles. The subject is allowed to use walking aids. The subject is asked how difficult the test was on a scale of 1 to 10.	12 months post-operative
Secondary	CT evaluation	CT scan will be done to assess the following anatomical items: Medial joint line position; Overall limb alignment; Joint obliquity; Rotation	6 weeks post-operative
Secondary	Power of knee flexion	Power of knee flexion via peak torque of quads measured on a digital myometer.	12 months post-operative
Secondary	Oxford Knee Score (OKS)	A questionnaire about your ability to perform daily functions.	12 months Post-operative
Secondary	Knee Injury and Osteoarthritis Score (KOOS)	A questionnaire to assess your ability to perform activities of different difficulty levels.	12 months Post-operative
Secondary	EuroQoL 5-dimension Health State (EQ-5D)	A questionnaire to assess your health and well-being.	12 months Post-operative
Secondary	Patient Satisfaction Score	A questionnaire to assess your satisfaction with your knee implant.	12 months Post-operative