Freedom® Total Knee System for Treatment of Osteoarthritis, Rheumatoid Arthritis or Post-traumatic Arthritis
Keywords
Abstract
Description
At all the clinical/telephonic follow-up visits i.e. at 8 weeks ± 1week, 1 year ± 1 month, 3 years ± 6 months, 5 years ± 6 months and 10 years ± 6 months implant survivorship and vital signs such as weight, heart rate etc including blood pressure will be recorded. Physical examination, lab measurements (optional), Radiographic assessment, concomitant medication/surgery and AE/SAE should be recorded. Also at all clinical follow ups OKS, KSS, range of motion will be recorded. The post-operative radiographic evaluations will be conducted at 0-8 weeks ± 1 week (which is considered as standard of care), 1 year ± 1 month, 3 years ± 6 months and optionally at 5 years ± 6 months, 10 years ± 6 months and Unscheduled visits, if required. The unscheduled visit is expected in some patients based on the fact that such patients might prone to complications like surgical site infections, venous thrombotic events, acute blood loss causing anaemia, nerve injury, and pain unresponsive to oral analgesics.
Dates
| Last Verified: | 06/30/2019 |
| First Submitted: | 01/22/2019 |
| Estimated Enrollment Submitted: | 07/23/2019 |
| First Posted: | 07/25/2019 |
| Last Update Submitted: | 02/13/2020 |
| Last Update Posted: | 02/16/2020 |
| Actual Study Start Date: | 02/29/2020 |
| Estimated Primary Completion Date: | 08/31/2024 |
| Estimated Study Completion Date: | 08/31/2032 |
Condition or disease
Intervention/treatment
Device: Freedom® Total Knee System
Phase
Arm Groups
| Arm | Intervention/treatment |
|---|---|
| Other: Freedom® Total Knee System A prospective, multi-centre, non-comparative, post-market clinical follow-up study to evaluate the survivorship, safety and performance of the Freedom® Total Knee System in United Kingdom | Device: Freedom® Total Knee System To evaluate the survivorship, safety and performance of the Freedom® Total Knee System in the treatment of subjects who in the surgeon's opinion require a primary total knee replacement due to severe knee joint pain and loss of mobility due to osteoarthritis, rheumatoid arthritis or post-traumatic arthritis. |
Eligibility Criteria
| Ages Eligible for Study | 18 Years To 18 Years |
| Sexes Eligible for Study | All |
| Accepts Healthy Volunteers | Yes |
| Criteria | Inclusion Criteria: - Male and female subjects aged between 18 years and 75 years. - Subjects who require unilateral knee prosthesis and have been evaluated as appropriate candidates for a total knee replacement by the investigator. - Subjects suffering from severe knee joint pain and loss of mobility due to rheumatoid arthritis, osteoarthritis or post-traumatic osteoarthritis. - Subjects, who in the opinion of the 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. - Subjects who are able to give voluntary, written informed consent to participate in this clinical investigation and from whom consent has been obtained. Exclusion Criteria: - Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this clinical investigation. - Subjects who are known drug or alcohol abuse or with psychological disorders that could affect follow-up care or treatment outcomes. - Subject with a known sensitivity to device materials. - Subjects with other significant disabling problems from the muscular-skeletal system other than in the knees (i.e muscular dystrophy, polio, neuropathic joints). - Subjects with a BMI of 40 or above. - Subjects with a current or active history of malignancy, active or suspected infection, Paget's disease, renal osteodystrophy, immunologically suppressed or have any other significant medical illness judged by investigator to exclude from study. - Subject with neuromuscular or neurosensory deficiency that may limit ability of the patient to evaluate the safety and efficacy of the device. - Female subjects who are pregnant or lactating. - Subjects who have previously undergone total or unicondylar knee replacement, high tibial osteotomy, ligament reconstruction, open reduction internal fixation (ORIF) or with previous fracture in the ipsilateral knee joint. |
Outcome
Primary Outcome Measures
1. Implant Survivorship Kaplan-Meier estimates of survivorship for all components [At 3 years]
Secondary Outcome Measures
1. Oxford Knee Score which consists of 12 questions [At 1 year and 3 years]
2. Range of Motion using a standard goniometer [At 1 year and 3 years]
3. Knee Society Score [At 1 year and 3 years]
